- Join our Health Care IT Courses. Exclusively for Health Care/ Life Sciences Graduates & Post Graduates
PHARMACOVIGILANCE
Pharmacovigilance is the science and activities relating to the detection, assessment, understanding, and prevention of adverse effects or any other medicine-related problem.
- Introduction to Pharmacovigilance (PV) Course curriculum.
- PV Career scope & PV Companies in India.
- Introduction to Pharmacovigilance (PV) Basics.
- PV Terminologies & Glossary.
- PV Websites.
- MedDRA Coding.
- ICH Guidelines (E2A to E2F).
- GVP Modules (1 to 16 Modules).
- Causality Assessment.
- Safety Narrative Writing (3 Types of Narratives, Spontaneous, Clinical Trial & Literature).
- Training on PV Database, PV Work Flows & Different software’s in PV Industry.
- Vaccine Pharmacovigilance.
- Materiovigilance (Medical Device).
3 Types :
Weekend Batch : 3 Months
Weekdays Batch : 2 Months
Crash Course : 1 Month (Only On Personal/Urgent Basis)
20000 RS for Indian Students.
25000 RS for NRI Students.
1. What is the Qualification For Pursuing the course:
B. Pharm, M. Pharm, Pharm. D, Ph. D, BDS, MDS, MBBS, BHMS, BAMS, B. PT
B. Sc (Nursing), M. Sc (Nursing).
2. Is this a certified course : Yes, you will be certified post completion of the course.
3. Average Pay Scale for Pharmacovigilance Job : From 13000 RS per month to 23000 RS/26000 RS depending
on the company from which you get the offer letter.
4. Process of Joining : Every month Rise Trainings conduct batches you can join by enrolling your name and sharing
the resume.
5. Is Placement or Job Assured for sure : Yes as long as you follow our 10 step method to achieve success.
We support the students with utmost care.
6. Training on Safety Database Present : Yes hands-on training on software is provided.
7. Can I pay the fee in installments : Yes, only two installments are permitted. One before joining and the
second before the course completion.
8. Payment of Fee Through : GPay/Phone Pe/Bank Account
9. How Is The Career Growth In Pharmacovigilance : Progressive & Prosperous.
10. Is there any abroad Opportunities For Pharmacovigilance : Yes, with good experience this chance of
abroad opportunities through the companies or through the experience you gained and doing masters would enable
more chances of getting good Pharmacovigilance jobs.
DRUG SAFETY PHYSICIAN COURSE PHARMACOVIGILANCE
Drug safety Physician and pharmacovigilance in areas of development and marketing of medication is an extremely important element. The importance of drug safety monitoring and risk management for medicinal product developers and clinical investigators is required to protect public health, manage increasingly tight regulations and ensure the efficient functioning of drug safety or pharmacovigilance systems within pharmaceutical and biotechnology companies.
- Medical review comments
- Relatedness assessment
- Listednes
- MedDRA coding
- Seriousness assessment IME and DME list
2 Types :
Weekdays Batch : 2 Months
Crash Course : 1 Month (Only On Personal/Urgent Basis)
35,000 RS for Indian Students
40,000 RS for NRI Students
1. What is the Qualification For Doing the course :
B. Pharm, M. Pharm, Pharm. D, Ph. D, BDS, MDS, MBBS, BHMS, BAMS, B. PT
B. Sc (Nursing), M. Sc (Nursing)
2. Is this a certified course : Yes, you will be certified post completion of the course.
3. Average Pay Scale for Drug Safety Physician Job : From33,000 RS per month to 37,000 RS/40,000 RS depending on the company from which you get the offer letter.
4. Process of Joining : Every month Rise Trainings conduct batches you can join by enrolling your name and sharing the resume.
5. Is Placement or Job Assured for sure : Yes as long as you follow our 10 step method to achieve success. We support the students with utmost care.
6. Training on Safety Database Present : Yes hands-on training on software is provided.
7. Can I pay the fee in installments : Yes, only two installments are permitted. One before joining and the second before the course completion.
8. Payment of Fee Through : GPay/Phone Pe/Bank Account
9. How Is The Career Growth In Drug Safety Physician : Progressive & Prosperous.
10. Is there any abroad Opportunities For Drug Safety Physician : Yes, with good experience this chance of abroad opportunities through the companies or through the experience you gained and doing masters would enable more chances of getting good Drug Safety Physician jobs.
CLINICAL DATA MANAGEMENT
Clinical data management (CDM) is a critical process in clinical research, which leads to the generation of high-quality,
reliable, and statistically sound data from clinical trials.
Module – 1:
Introduction to Clinical Research and Clinical Data Management
Roles & Responsibilities of Key Stakeholders.
Standard Operating Procedures.
Study Set-up Phase :
Module – 2:
Creation of Study set-up documents
Protocol Orientation.
Preparation of DMP/DHP.
CRF Design.
Preparation of DVP.
CRF Annotation.
DB-Design and Set-up.
User acceptance test.
Third party data specifications and testing.
Coding Specifications and testing.
SAE Reconciliation specifications.
Self Evident Correction specifications.
Custom reports specifications.
Study Conduct phase :
Module – 3:
Study Ongoing phaset
Tracking CRF Data.
Data Entry, Remote Data Entry.
Data review and query management.
Managing Lab Data.
Medical Coding.
SAE Reconciliation.
Post-Production Change management (PPC).
Self Evident Correction Management (SEC).
Creating Reports .
Study Close-out phase :
Module – 4:
Study Close out phase
DB listings QC as per QC plan.
Track all data as per DB Lock checklist.
Final DB QC.
Data Base Lock.
Data Base archival and study data transfer.
Module – 5:
Case Studies
2 Types :
Weekdays Batch : 2 Months
Crash Course : 1 Month (Only On Personal/Urgent Basis)
20,000 RS for Indian Students.
25,000 RS for NRI Students.
1. What is the Qualification For Doing the course :
B. Pharm, M. Pharm, Pharm. D, Ph. D, BDS, MDS, MBBS, BHMS, BAMS
B. PT, B. Sc (Nursing), M. Sc (Nursing)
2. Is this a certified course : Yes, you will be certified post completion of the course.
3. Average Pay Scale for Clinical data management (CDM) Job: From 13000 RS per month to 23000 RS/26000 RS depending
on the company from which you get the offer letter.
4. Process of Joining : Every month Rise Trainings conduct batches you can join by enrolling your name and sharing
the resume.
5. Is Placement or Job Assured for sure : Yes as long as you follow our 10 step method to achieve success.
We support the students with utmost care.
6. Training on Safety Database Present : Yes hands-on training on software is provided.
7. Can I pay fee in installments : Yes, only two installments are permitted. One before joining and the second
before the course completion.
8. Payment of Fee Through : GPay/Phone Pe/Bank Account
9. How Is The Career Growth In Clinical data management (CDM) : Progressive & Prosperous.
10. Is there any abroad Opportunities For Clinical data management (CDM) : Yes, with good experience this chance of
abroad opportunities through the companies or through the experience you gained and doing masters would enable more
chances of getting good Clinical data management (CDM) jobs.
CLINICAL RESEARCH
Clinical research is a branch of healthcare science that determines the safety and effectiveness of medications, devices,
diagnostic products and treatment regimens intended for human use.
- Introduction to CR – 2 hrs
a) Definitions and types of CR.
b) Overview of CR processes.
c) Opportunities in CR.
d) Career Development in CR.
- BA/BE studies-Clinical and Regulatory procedures-ANDA-21 CFR 320 – 4 hrs.
- CRO-Organization, Structure, Role, Responsibilities, Costing – 4 hrs.
- Contracts and Agreements—CDA, MSA, CTA – 2 hrs.
- Insurance and Indemnity – 1 hr.
- Overview of SOPs/Study Plans – 2 hrs
- Overview of Protocol, ICF, IB, AEs – 3 hrs
Responsibilities:
- Sponsor/Investigator/EC – 4 hrs
- Phases of Clinical Trials – 2 hrs
- Clinical Trial Management-ICH GCP – 4 hrs
Clinical Trial Procedures:
- Budgeting, Medical Writing, IM, SIV, SMV, SCV – 4 hrs.
- CT-Regulatory- Indian Forms as per CDSCO-# 44, 45, 12, 11 – 2 hrs
- US-Forms-1571, 1572, 3454, 3455 – 2 hrs
- CT-Regulatory Procedures-India-Schedule Y – 4 hrs
- US-21 CFR part 50, 54, 56, 312, 314 – 4 hrs
- EU-EMEA, Australia-TGA, UK-MHRA, Canada-HPFB, Japan – 4 hrs
- All CR related Forms-AE, SAE, Subject ID code list, Staff Delegation log, etc – 4 hrs
- Audits and Inspections: Overview-Quality systems and SOPs – 2 hrs
Audits and Inspections:
- Overview-Quality systems and SOPs – 4 hrs
- Medical Devices-PMA, similarities and differences between Medical Devices and Drugs – 2 hrs
2 Types :
Weekdays Batch : 2 Months
Crash Course : 1 Month (Only On Personal/Urgent Basis)
20,000 RS for Indian Students.
25,000 RS for NRI Students.
1. What is the Qualification For Doing the course :
B. Pharm, M. Pharm, Pharm. D, Ph. D, BDS, MDS, MBBS, BHMS, BAMS
B. PT, B. Sc (Nursing), M. Sc (Nursing)
2. Is this a certified course : Yes, you will be certified post completion of the course.
3. Average Pay Scale for Clinical research Job : From 13000 RS per month to 23000 RS/26000 RS depending on the company
from which you get the offer letter.
4. Process of Joining : Every month Rise Trainings conduct batches you can join by enrolling your name and sharing the
resume.
5. Is Placement or Job Assured for sure : Yes as long as you follow our 10 step method to achieve success. We support
the students with utmost care.
6. Training on Safety Database Present : Yes hands-on training on software is provided.
7. Can I pay the fee in installments : Yes, only two installments are permitted. One before joining and the second
before the course completion.
8. Payment of Fee Through : GPay/Phone Pe/Bank Account
9. How Is The Career Growth In Clinical research : Progressive & Prosperous.
10. Is there any abroad Opportunities For Clinical research : Yes, with good experience this chance of abroad
opportunities through the companies or through the experience you gained and doing masters would enable more chances
of getting good Clinical research jobs.
CLINICAL SAS
Statistical Analysis System, or SAS, has been the industry standard for data management and analytics of large volumes of data. It’s a very flexible platform that provides users with various means to manipulate, analyze, process, and report on data.
- BASE SAS PROGRAMMING
1. Introduction to SAS Programming in clinical research
2. Exploring SAS Profile creation and SAS credentials creation, SAS STUDIO
3. Understanding SAS datasets, SAS syntax, types of variables and attributes, resolving erros / check
logs
4. Accessing data through libraries, how to create libraries, Import / export data (CSV, XML, TAB,
TXT)
5. Importing data using Datastep ( infile , datalines ) . Methods of reading data into sas
6. Understanding PDV in importing and generating datasets
7. Create your data using datastep , where , keep , drop , rename options
8. Functions – Numeric
9. Function – Date
10. Funtions – Character
11. Special functions
12. Sub setting data using where / If conditions along with manipulating functions
13. Proc format
14. Proc sort, removing duplicates, first., last.
15. Running totals, Output statement, do loop intro
16. Do loops
17. Arrays
18. Setting data vertically
19. Merging data
20. Proc transpose of data, remerging concept and structuring data
21. Proc freq , proc means , proc tabulate , proc print , proc Univariate
22. Proc compare, validating data
23. Proc report, ods, putlog - ADVANCE SAS PROGRAMMING:
1. Introduction to SAS SQL Procedure
2. Comparing SAS vs SQL process
3. How to use functions in SQL, Where conditions in SQL
4. Summarizing and Grouping Data, group by, having, calculated option
5. Using DICTIONARY Tables
6. Creating and Managing Tables
7. SQL Joins
8. Subqueries
9. Inline views
10. Set operators
11. Creating macros in SQL, what are macros? Why?
12. Program Flow in macros
13. Explaining Macro facility and what are types of macro variables and scope
14. Creating macros using different parameters
15. Creating macro variables (local, global)
16. Creating macros using SQL, creating macros using dataset (Call symput routing)
17. Macro functions
18. Resolution of macros and understanding macro nesting
19. Indirect referring of macros – Forward rescan rule
20. Conditional processing of macros
21. Iterative processing of macros
22. Generating data dependant macro snippet – an example for dynamic coding process - CDISC PROJECT – OPTIONAL COURSE – END TO END PROCESS EXPLANATION
1. CRF ANNOTAION OVERVIEW
2. Understanding PROTOCOL, SAP, MOCK SHELLS / Clinical research documents.
3. SDTM DOMAIN PROGRAMMING
• TA
• TE
• TI
• TS
• TV
• DM
• DS
• EX
• LB
• CM
• AE
• EG
• SUPPDM - ADAM PROGRAMMING:
• ADAE
• ADCM
• ADSL
• ADAE
• ADLB - TFL PROGRAMMING
• SAFETY LISTINGS
• SAFETY TABLES
• SAFETY GRAPHS - NOTE: BASE AND ADVANCE PROGRAMMING FOR 45 DAYS (1 Hour/ Day)
PROJECT – 15 DAYS OF CLASSES 1 hours / Day and Weekly connects for any additional help in
working on assigned deliverables
Official SAS TRAINING MODULES will be given as study materials , along with Case studies and
daily email handouts will be provided along with Live Sessions which can be recorded.
2 Types :
Weekdays Batch : 2 Months
Crash Course : 1 Month (Only On Personal/Urgent Basis)
35,000 RS for Indian Students.
40,000 RS for NRI Students.
1. What is the Qualification For Doing the course :
B. Pharm, M. Pharm, Pharm. D, Ph. D, BDS, MDS, MBBS, BHMS, BAMS, B. PT
B. Sc (Nursing), M. Sc (Nursing)
2. Is this a certified course : Yes, you will be certified post completion of the course.
3. Average Pay Scale for Clinical SAS Job : From 26000 RS per month to 33000 RS/36000 RS depending on the company from which you get the offer letter.
4. Process of Joining : Every month Rise Trainings conduct batches you can join by enrolling your name and sharing the resume.
5. Is Placement or Job Assured for sure : Yes as long as you follow our 10 step method to achieve success. We support the students with utmost care.
6. Training on Safety Database Present : Yes hands-on training on software is provided.
7. Can I pay the fee in installments : Yes, only two installments are permitted. One before joining and the second before the course completion.
8. Payment of Fee Through : GPay/Phone Pe/Bank Account
9. How Is The Career Growth In Clinical SAS : Progressive & Prosperous.
10. Is there any abroad Opportunities For Clinical SAS : Yes, with good experience this chance of abroad opportunities through the companies or through the experience you gained and doing masters would enable more chances of getting good Clinical SAS jobs.
eTMF MODULE
eTMF Model is a supported initiative of the Drug Information Association’s (DIA) Document and Records Management Community and represents a single, unified interpretation of the regulations and best practices related to Trial Master Files that would be accepted by all clinical trial stakeholders, with a view to being adaptable and adopted by any organization.
1. Introduction to Essential Documents
2. Introduction DIA eTMF reference model
3. eTMF Mangement Plan
4. eTMF tools description
5. eTMF EDL creation
6. eTMF conduct
7. eTMF review
8. eTMF reconcilliation
9. eTMF document upload
10. eTMF document completion guidelines
11. eTMF demo -Viva Vault
12. eTMF demo – general systems
13. eTMF filling guidelines
14. Assessments -1
15. Mock Interview Questions
15 hours Classroom/Online Training
35,000 RS for Indian Students.
40,000 RS for NRI Students.
1. What is the Qualification For Doing the course : B. Tech, B. Pharm, M. Pharm, Pharm. D, Ph. D, BDS, MDS, MBBS, BHMS, BAMS
B. PT, B. Sc (Nursing), M. Sc (Nursing)
2. Is this a certified course : Yes, you will be certified post completion of the course.
3. Average Pay Scale for eTMF Module : From 15000 RS per month to 18000 RS/23000 RS depending on the company from which you get the offer letter.
4. Process of Joining : Every month Rise Trainings conduct batches you can join by enrolling your name and sharing the resume.
5. Is Placement or Job Assured for sure : Yes as long as you follow our 10 step method to achieve success. We support the students with utmost care.
6. Training on Safety Database Present : Yes hands-on training on software is provided.
7. Can I pay the fee in installments : Yes, only two installments are permitted. One before joining and the second before the course completion.
8. Payment of Fee Through : GPay/Phone Pe/Bank Account
9. How Is The Career Growth In eTMF Module : Progressive & Prosperous.
10. Is there any abroad Opportunities For eTMF Module : Yes, with good experience this chance of abroad opportunities through the companies or through the experience you gained and doing masters would enable more chances of getting good eTMF Module Jobs.
CTD/eCTD REGULATORY AFFAIRS BASICS
CTD/eCTD Regulatory Affairs is the standard format for submitting applications, amendments, supplements, and reports to FDA’s Center for Drug Evaluation and Research (CDER) and Center for Biologics Evaluation and Research (CBER).
1. Introduction to RA profession
Regulatory Affairs Profession, role and its importance, overview of worldwide Regulatory agencies
General Overview of the Pharmaceutical Industry, its functioning, role of various Departments
like R & D, Production, RA, QA, Project Management, Supply chain etc. Within the industry
2. ICH and CTD
Overview of ICH
Introduction and overview of CTD
3. Organization of CTD
Module 1. Administrative and Prescribing Information
(Region specific)
Module 2. Common Technical Document Summaries
Module 3: “QUALITY” – CMC section of the CTD
Module 4: Nonclinical study reports
Module 5: Clinical study reports
4. Introduction to eCTD
Need to Harmonize
Origin of CTD
CTD Modules
Introduction to eCTD
Document Granularity
Advantages of eCTD
Need of eCTD Builder Software
DTD
Index.xml File
Regional xml File
USFDA
- Admin Information in US-regional.xml
- File Formats supported in eCTD for USFDA
- PDF Specification for USFDA
Folder Structure
STF (Study Tagging File)
RSN Concept
Way to submit the Final Submission
Things to be taken care while preparing eCTD submission
15 hours Classroom/Online Training
20,000 RS for Indian Students.
25,000 RS for NRI Students.
1. What is the Qualification For Doing the course : B. Tech, B. Pharm, M. Pharm, Pharm. D, Ph. D, BDS, MDS, MBBS, BHMS, BAMS
B. PT, B. Sc (Nursing), M. Sc (Nursing)
2. Is this a certified course : Yes, you will be certified post completion of the course.
3. Average Pay Scale for CTD/eCTD Regulatory Affairs : From 25000 RS per month to 30000 RS/35000 RS depending on the company from which you get the offer letter.
4. Process of Joining : Every month Rise Trainings conduct batches you can join by enrolling your name and sharing the resume.
5. Is Placement or Job Assured for sure : Yes as long as you follow our 10 step method to achieve success. We support the students with utmost care.
6. Training on Safety Database Present : Yes hands-on training on software is provided.
7. Can I pay the fee in installments : Yes, only two installments are permitted. One before joining and the second before the course completion.
8. Payment of Fee Through : GPay/Phone Pe/Bank Account
9. How Is The Career Growth In CTD/eCTD Regulatory Affairs : Progressive & Prosperous.
10. Is there any abroad Opportunities For CTD/eCTD Regulatory Affairs : Yes, with good experience this chance of abroad opportunities through the companies or through the experience you gained and doing masters would enable more chances of getting good CTD/eCTD Regulatory Affairs Jobs.
CTD/eCTD REGULATORY AFFAIRS ADVANCED
CTD/eCTD Regulatory Affairs is the standard format for submitting applications, amendments, supplements, and reports to FDA’s Center for Drug Evaluation and Research (CDER) and Center for Biologics Evaluation and Research (CBER).
1. Introduction to RA profession
Regulatory Affairs Profession, role and its importance, overview of Worldwide Regulatory agencies.
General Overview of the Pharmaceutical Industry, its functioning, role of various departments like R & D, Production, RA, QA, Project Management, Supply chain, etc. within the industry
2. Overview of Drug Development Process
New Drug Approval and Development
Preclinical Investigation
Investigational New Drug Application (INDA)
Clinical Investigation
New Drug Application (NDA)
Phase IV (Post marketing Surveillance)
Importance of Pharmacovigilance,
EVMPD and XEVMPD
3. Formulation or Product development
Basic formulation development and manufacturing
Importance of preformulation studies and planning
PDR writing as per ICH Q8
4. GMP , GLP and GCP
Overview of GMP
Overview of GLP
Overview of GCP
ICH GCP Guidance’s and its importance
ICH E3, ICH E6
Importance of PIC/S
5. Regulatory System in US (FDA)
History of FDA and Related Regulatory Agencies
FDA & CDER – Organization and responsibilities
Types of Drug applications in US [IND, NDA, ANDA, 505 (b)(2)]
Investigational New Drug Application: INDA
New Drug Application: NDA
Generic Drug Submissions
ANDA submission in detail
Bioequivalence Recommendation for Specific Products
Establishment registration, drug registration and National Drug Code Directory (NDC)
Changes to an approved ANDA and annual reporting
Over-the-Counter Drug Products
Regulation of OTC Drugs
Rx-to-OTC Switch
Patents and Exclusivity
Prescription Drug Labeling, Advertising and Promotion
Labeling Regulations and Requirements
Structured Product Labeling (SPL)
6. Biologics Submissions
IND Process for Biologics
Preclinical Development Considerations for Biologics
Clinical Development Considerations for Biologics
Manufacturing of Clinical Trial Material for Biologics
BLA Format and Content
BLA Review Process
Biosimilars
Vaccines and Related Biological Products
7. Drug Substance Registration Drug Master Files (DMF)
Type I —Reserved, no longer applicable
Type II — Drug substance, drug substance intermediate and material used in their preparation, or drug product
Type III — Packaging material
Type IV — Excipients, colorant, flavor, essence or material used in their preparation
Type V — FDA accepted reference material
COS/CEP
ASF
8. Life Cycle of Drug Product
Prior Approval Supplement (PAS)
Post Approval Changes [SUPAC]
Changes Being Effected in 30 Days (CBE-30)
Annual Report
Post marketing Reporting Requirements
Post approval Labeling Changes
Lifecycle Management
FDA Inspection and Enforcement Act
Form FDA 483
Establishment Inspection Report (EIR)
Warning Letters
Recalls, Seizure and Injunctions
9. Regulatory System in Canada (Health Canada)
New Drug Approval Process
Generic Drug Approval Process
10. Regulatory System in Europe (EMA)
Pharmaceuticals in the European Union
History of Drug Regulation in European Countries
Centralized Regulatory Authority of European Union (EU)
EUDRALEX: EU Pharmaceutical Legislation
European Medicines Agency (EMA)
Regulation of medicines in the European Union
Marketing Authorization
Centralized Procedure (CP)
Mutual Recognition Procedure (MRP)
Decentralized Procedure (DCP)
National Procedure
Types of Variations
11. Drug Registration with Rest of the World (ROW)
Introduction and Overview of Row regions and sub-regions
Registration with South-East Asian countries (ASEAN)
Registration with Latin America (Brazil, Mexico),
Registration with Middle East countries (GCC)
Registration in Emerging market (India, Russia, China, Japan, South Africa)
12. Dossier Preparation-Different Formats used Globally-
pCTD [Paper- CTD]
eCTD [Electronic CTD]
ACTD [ASEAN CTD]
NeeS [Non eCTD Electronic Submission]
13. Dossier preparation in pCTD and eCTD format
Introduction and Overview
CTD Format for Each Submission (US/EU)
Module 1 – Administrative and Prescribing Information
Module 2 – Common Technical Document Summaries
Module 3 – Quality Part-CMC
Module 4 – Nonclinical Study Reports
Module 5 – Clinical Study Reports
Electronic Submission
Planning your electronic submission
Regulatory requirements
Tool and Technologies Electronic Submission Process
NeeS: Non eCTD electronic Submission
· eCTD: Electronic submissions with xml backbone files
Electronic Submission Gateway (ESG)
14. Dossier preparation in ACTD format
Introduction and Overview
ACTD Format for ASEAN countries
PART-I – Administrative and Prescribing Information
PART-II – Quality Part-CMC
PAR-III – Nonclinical Study Reports
PART-IV – Clinical Study Reports
15. ICH Quality Guidance’s and its importance
Overview of –
ICH Q1 – Stability studies
ICH Q2 – Analytical Method Validation
• ICH Q3 – Impurities
• ICH Q4 – Pharmacopoeias
ICH Q5 – Quality of Biotechnological Products
• ICH Q6 – Specifications
ICH Q7 – Good Manufacturing Practice
ICH Q8 – Pharmaceutical Development
ICH Q9 – Quality Risk Management
ICH Q10 – Pharmaceutical Quality system
ICH Q11 – Development and Manufacture of Drug Substances(QbD)
16. 21CFR Part 11 guidance and its importance
17. Abbreviations
15 hours Classroom/Online Training
20,000 RS for Indian Students.
25,000 RS for NRI Students.
1. What is the Qualification For Doing the course : B. Tech, B. Pharm, M. Pharm, Pharm. D, Ph. D, BDS, MDS, MBBS, BHMS, BAMS
B. PT, B. Sc (Nursing), M. Sc (Nursing)
2. Is this a certified course : Yes, you will be certified post completion of the course.
3. Average Pay Scale for eCTD/CTD : From 15000 RS per month to 20000 RS/23000 RS depending on the company from which you get the offer letter.
4. Process of Joining : Every month Rise Trainings conduct batches you can join by enrolling your name and sharing the resume.
5. Is Placement or Job Assured for sure : Yes as long as you follow our 10 step method to achieve success. We support the students with utmost care.
6. Training on Safety Database Present : Yes hands-on training on software is provided.
7. Can I pay the fee in installments : Yes, only two installments are permitted. One before joining and the second before the course completion.
8. Payment of Fee Through : GPay/Phone Pe/Bank Account
9. How Is The Career Growth In eCTD/CTD : Progressive & Prosperous.
10. Is there any abroad Opportunities For eCTD/CTD : Yes, with good experience this chance of abroad opportunities through the companies or through the experience you gained and doing masters would enable more chances of getting good eCTD/CTD Jobs.
CERTIFICATION IN MEDICAL CODING — CMC
CMC Training Program
CMC – A Complete Job Oriented Training Program
CMC Certification is provided to candidates after attending 66 hours of training and clearing the various test conducted in the training program.
CMC is a job oriented training program covering all topics in Anatomy, Physiology and Pathology and ICD-10 CM, Basics of CPT-4 and HCPCS Coding.
✔ Anatomy, Physiology & Pathology Training Manual – Included
✔ Certification in Medical Coding Training Manual – Included
Topics Covered:
✔ Medical Terminology.
✔ Complete Anatomy, Physiology, Pathology, Clinical tests and Surgical Procedures.
✔ ICD-10 CM General Coding guidelines, conventions and coding for acute and chronic conditions and late effect, Impending and Pressure ulcer stages Coding.
✔ ICD- 10 CM Chapter Specific Guidelines including all the chapters like Fracture, Laceration, Poisoning Coding
✔ Introduction CPT-4 Procedure Coding Terminologies, HCPCS and Modifiers Coding.
✔ HIPAA Training.
✔ Revenue Cycle Management and CPC, CPC-A and CCS-P sample question pattern
Salient Features of CMC
✔ Comprehensive Training focused on Job Training and Placement.
✔ Complete ICD-10 CM Coding with Detailed Exposure to General Coding Guidelines and Chapter Specific Guidelines’ training with HIPAA compliance.
✔ CPT4 Procedural Coding, HCPCS and Modifiers Coding and RCM training with HIPAA compliance.
✔ Training methodologies and Placement process is in par with ISO 9001:2008 certification standards.
✔ Anatomy and Physiology training through plenty of videos.
✔ Certification provided after successful completion of Coding Training
✔ Interview Training.
✔ Placement assurance after certification.
Course Duration : 45 Hours
Batches : Weekdays and Weekend Batch
Weekdays : Monday to Friday
Weekends : Saturday & Sunday
25,000 RS for Indian Students.
30,000 RS for NRI Students.
1. What is the Qualification For Doing the course : B. Tech, B. Pharm, M. Pharm, Pharm. D, Ph. D, BDS, MDS, MBBS, BHMS, BAMS
B. PT, B. Sc (Nursing), M. Sc (Nursing)
2. Is this a certified course : Yes, you will be certified post completion of the course.
3. Average Pay Scale for Argus Medical Coding : From 30000 RS per month to 33000 RS/35000 RS depending on the company from which you get the offer letter.
4. Process of Joining : Every month Rise Trainings conduct batches you can join by enrolling your name and sharing the resume.
5. Is Placement or Job Assured for sure : Yes as long as you follow our 10 step method to achieve success. We support the students with utmost care.
6. Training on Safety Database Present : Yes hands-on training on software is provided.
7. Can I pay the fee in installments : Yes, only two installments are permitted. One before joining and the second before the course completion.
8. Payment of Fee Through : GPay/Phone Pe/Bank Account
9. How Is The Career Growth In Medical Coding : Progressive & Prosperous.
10. Is there any abroad Opportunities For Medical Coding : Yes, with good experience this chance of abroad opportunities through the companies or through the experience you gained and doing masters would enable more chances of getting good Medical Coding Jobs.
MEDICAL COMMUNICATIONS
Medical communications are designed to stimulate awareness, discussion and procurement of new medical devices, drugs and treatments. Aimed at healthcare practitioners, buyers and stakeholders, it is a key aspect of pharmaceutical marketing.
Our training program includes the following components:
Audit of writing skills
About Medcomm Agencies
Blog articles
Infographics
Manuscript Writing
Tool and technique in Medical Writing
Detailing aids
Leave Behind Literature
Case reports
Advisory Board Meeting
Consensus document
Patient Education
Slide Kits – Training Modules
Slide Kits – Speaker Presentations
Post-meeting deliverables
KOL related communications
Insights/SMP/USP/Copywriting
White Papers
Freelancing
Networking
The program is covered in 9 sessions where you will be introduced to the practical aspects of medical writing over a period of 3 months.
The consultation fees is INR 15,000 for a group session.
1. What is the Qualification For Doing the course:
B.E, B. Tech, MCA, M. Tech.
2. Is this a certified course : Yes, you will be certified post completion of the course.
3. Average Pay Scale for AWS Job : From 25000 RS per month to 30000 RS/35000 RS depending on the company from which you get the offer letter.
4. Process of Joining : Every month Rise Trainings conduct batches you can join by enrolling your name and sharing the resume.
5. Is Placement or Job Assured for sure : Yes as long as you follow our 10 step method to achieve success. We support the students with utmost care.
6. Training on Safety Database Present : Yes hands-on training on software is provided.
7. Can I pay the fee in installments : Yes, only two installments are permitted. One before joining and the second before the course completion.
8. Payment of Fee Through : GPay/Phone Pe/Bank Account
9. How Is The Career Growth In AWS : Progressive & Prosperous.
10. Is there any abroad Opportunities For AWS : Yes, with good experience this chance of abroad opportunities through the companies or through the experience you gained and doing masters would enable more chances of getting good AWS jobs.
HEALTH ECONOMICS AND OUTCOMES RESEARCH (HEOR)
HEOR is a field of research that uses economic data to evaluate the value of healthcare interventions, including pharmaceuticals. It can be used to determine the cost-effectiveness of treatments by comparing their costs and benefits.
S.No | Session number | Topics to be delivered |
1 | Session – I | Introduction HEALTH ECONOMICS AND OUTCOMES RESEARCH (HEOR) |
2 | Session – II | Research Methodology and Study Designs |
3 | Session – III | Introduction to Systematic Literature Review (SLR) – Part I |
4 | Session – IV | Key concept and steps involved in SLR – Part II |
5 | Session – V | Critical appraisal (Why/how to perform it and its importance) in SLR |
6 | Session – VI | SLR (Clinical) |
7 | Session – VII | Pharmacoeconomics and Economic Evaluation Methods (EEM) |
8 | Session – VIII | Patient-reported outcomes (PROs) |
9 | Session –IX | Introduction to Health Technology Assessments (HTAs) agencies and its role |
10 | Session – X | Introduction to Bio-statistics |
11 | Session – XI | Key concepts of Bio-statistics in HEOR |
12 | Session – XII | PubMed interface training superficially for how to retrieve the relevant studies |
The consultation fees is INR 15,000 for Weekend Batches only.
The program is covered over a period of 3 months