Concept → demonstration → practice → validation → QC.
Healthcare & Life Sciences Training Academy
Build Your Career in Healthcare & Life Sciences
Industry-focused training in Clinical Research, Pharmacovigilance, Clinical Data Management, Medical Coding, Medical Writing, Regulatory Affairs, Clinical SAS/CDISC and more.
11Career Tracks
158Classes
316Approx. Core Hours
12+Years Combined Experience*
*Use this experience claim only if it is factually verifiable for the team/academy.
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CAREER TRACK
Medical Coding
30 Classes • ICD-10-CM • CPT • HCPCS • QC
Learning pathwayCareer-ready
Learn
Foundation & terminology
Practice
Workflow & cases
Validate
Errors, QC & review
Prepare
Portfolio & interviews
Each major track includes the foundation required to begin.
Assignments, scenarios, capstones and portfolio artifacts.
Resume, role-based questions, mock interview and job-search support.
About MEDICODE
Training designed around how healthcare work is actually done.
MEDICODE is a healthcare and life-sciences training academy focused on preparing students and professionals for industry roles across Clinical Research, Pharmacovigilance, Clinical Data Management, Medical Coding, Medical Writing, Medical Scribing, Regulatory Affairs and Clinical SAS/CDISC.
Our learning model combines strong domain foundations with workflow-based training, practical cases, software exposure, quality checks, assignments, capstone activities and interview preparation.
Independent career tracks
Recognized professional terminology
Practical cases & assignments
Software-linked learning
QC, troubleshooting & validation
Career and interview support
THE MEDICODE METHOD
Learn → Practice → Validate → Present
01
Foundation
Build domain vocabulary, regulations, systems and professional context.
02
Workflow
Understand the inputs, rules, fields, outputs and stakeholder handoffs.
03
Practical Execution
Work with case exercises, source documents and guided simulations.
04
Quality & Career Readiness
Review errors, perform QC and explain decisions confidently in interviews.
11 Independent Career Tracks
Choose the track that matches your career goal.
Each course is presented by class count instead of day ranges, making duration clear for students and counsellors.
01
20 Classes
Clinical Trial Management
GCP, protocols, site start-up, monitoring, CTMS/eTMF, risk/CAPA, vendors, recruitment and closeout.
GCPCTMSeTMF
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02
18 Classes
Clinical Data Management
Protocol review, CRF/eCRF, EDC, edit checks, queries, reconciliation, data review and database lock.
EDCCRFQueries
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03
20 Classes
Pharmacovigilance / Drug Safety
ICSR processing, MedDRA, WHODrug, narratives, causality, reporting, signals and literature surveillance.
ICSRMedDRAWHODrug
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04
13 Classes
Medical Writing
Protocol, IB, CSR, safety writing, publications, literature search, patient-facing writing, CTD summaries and QC.
CSRProtocolPublications
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05
4 Classes
Professional Communication & Soft Skills
Professional English, business documentation, ATS resume, LinkedIn, interview readiness and workplace communication.
ATSLinkedInInterview
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POPULAR
06
30 Classes
Medical Coding
US healthcare, RCM, anatomy, ICD-10-CM, CPT, HCPCS, E/M, modifiers, coding edits, audit/QC and CPC-style preparation.
ICD-10-CMCPTHCPCS
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07
12 Classes
Medical Scribing
HPI/OPQRST, ROS, SOAP, EHR workflow, privacy/HIPAA awareness, telehealth and AI-assisted documentation review.
EHRSOAPClinical Notes
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08
16 Classes
Regulatory Affairs
Global agencies, ICH/GxP, submission pathways, CTD/eCTD, lifecycle management, RIM and publishing awareness.
ICHCTDeCTD
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09
18 Classes
Clinical SAS & CDISC
SAS programming, SQL, macros, SDTM, ADaM, TLFs, Define-XML, validation, programming QC and submission readiness.
SASSDTMADaM
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10
4 Classes
PV Systems & Software
Safety-system workflow, roles, case versioning, audit trails, E2B(R3), dashboards, signal tools and regulatory gateways.
E2B(R3)Safety DBSignals
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11
3 Classes
eCTD Submission & Publishing Software
Sequence assembly, metadata, lifecycle, publishing, technical validation, error resolution and archival evidence.
eCTDPublishingValidation
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Integrated Master Catalogue
158 Classes. 11 Career Tracks. One structured learning ecosystem.
The complete catalogue combines independent professional tracks with approximately 316 instructor-led core hours, plus additional practical/lab exercises where applicable.
158Classes
316Approx. Core Hours
11Career Tracks
4Learning Stages
Student Outcomes
What will students learn?
Training combines domain knowledge, source interpretation, workflow execution, software concepts, QC and career readiness.
Domain Foundation
Build professional vocabulary, healthcare context and role-specific fundamentals.
Source Interpretation
Read protocols, charts, CRFs, safety reports, clinical notes, datasets and submission documents.
Industry Workflows
Understand input → execution → validation → QC → output sequences.
Software Exposure
Navigate simulations or demonstrations of role-specific industry systems where applicable.
Standards & Terminology
Use recognized professional standards and controlled terminology relevant to the chosen track.
Error Handling
Identify common errors, troubleshoot issues and understand escalation paths.
Quality & Compliance
Perform consistency checks, validation and role-appropriate quality review.
Projects & Portfolio
Complete assignments, case-based exercises and capstone artifacts.
Interview Readiness
Prepare for technical, scenario-based and HR interview conversations.
Systems & Tools
Learn the workflows behind industry systems.
Exposure is course-specific and may be hands-on/simulated, workflow demonstration or industry awareness depending on licensed access.
Clinical Research
CTMS • eTMF • EDC • IRT/RTSM • eCOA
Drug Safety
Safety Databases • MedDRA • WHODrug • Signal Tools
Medical Coding
ICD-10-CM • CPT • HCPCS • Encoder/CAC
Medical Scribing
EHR Workflow • Clinical Documentation • Speech/AI Awareness
Clinical Programming
SAS • SDTM • ADaM • Define-XML • Validation
Regulatory & eCTD
RIM • eCTD Publishing • Lifecycle • Validation
Why MEDICODE
Designed for understanding, execution and confidence.
Industry-Aligned Learning
Structured around recognized terminology, regulations, coding systems and professional workflows.
Practical & Workflow-Based
Source documents, cases, system simulations, error handling, quality checks and capstones.
Independent Career Tracks
Major tracks include their own foundation so students can choose a focused pathway.
Career Preparation
Resume/ATS, LinkedIn positioning, interview questions, mock practice and job-search support.
Career Readiness & Placement Assistance
Training should end with a confident next step.
Career support focuses on presenting your skills clearly, preparing for role-based interviews and helping you navigate the job-search process.
- ATS-focused resume building
- LinkedIn optimization
- Technical and HR mock interviews
- Scenario-based interview preparation
- Portfolio presentation guidance
- Job-search and application support
Placement assistance supports the job-search process; employment outcomes depend on eligibility, performance, market conditions and employer selection.
CAREER WORKFLOW
01Build SkillsDomain + practical foundation
02Build EvidenceCases + portfolio artifacts
03Build ProfileResume + LinkedIn
04Build ConfidenceMock interviews + scenarios
India & international career pathways
A world of opportunities in clinical research.
Explore the industries and organizations connected to clinical research and life sciences.
CROs & clinical trial services
Trial coordination, site activation, monitoring and trial documentation.
Pharmaceutical companies
Clinical development, drug safety, regulatory operations and medical writing.
Biotechnology & vaccines
Biologic development, clinical operations and safety support.
Hospitals & trial sites
Study coordination, participant follow-up and research documentation.
Research institutes & academia
Project research, study data collection and research administration.
Clinical data & technology services
Clinical data management, statistical programming and research analytics.
Medical devices & diagnostics
Clinical investigations, evidence generation and vigilance.
Specialist safety & writing services
ICSR processing, safety operations, scientific and regulatory writing.
Employer discovery
Get application supportExplore organizations in India and around the world
Career research directory, not a placement-partner list. These examples do not claim MEDICODE alumni placements, recruitment partnerships or endorsements. The directory is representative, not exhaustive. Vacancies, qualifications, experience and work authorization vary; check each organization’s official site.
22 organizations
India-based
Syngene International
CRO & research services
Official website ↗India-basedCliantha Research
CRO & clinical studies
Official website ↗India-basedVeeda Lifesciences
Clinical & preclinical research
Official website ↗India-basedLambda Therapeutic Research
CRO & clinical studies
Official website ↗India-basedSIRO Clinpharm
Clinical research services
Official website ↗India-basedSun Pharma
Pharmaceutical industry
Official website ↗India-basedDr. Reddy’s Laboratories
Pharmaceutical industry
Official website ↗India-basedBiocon
Biopharmaceutical industry
Official website ↗India-basedICMR & its institutes
Public research institutions
Official website ↗India-basedTata Memorial Centre / ACTREC
Hospital & oncology research
Official website ↗India-basedAIIMS Rishikesh
Hospital & academic research
Official website ↗International / globalIQVIA
Clinical research & analytics
Official website ↗International / globalICON
Global CRO
Official website ↗International / globalParexel
Global CRO
Official website ↗International / globalMedpace
Global CRO
Official website ↗International / globalThermo Fisher Scientific / PPD
Clinical research & laboratories
Official website ↗International / globalFortrea
Global CRO
Official website ↗International / globalSyneos Health
Clinical development services
Official website ↗International / globalWorldwide Clinical Trials
Global CRO
Official website ↗International / globalNovartis
Pharmaceutical & clinical development
Official website ↗International / globalPfizer
Pharmaceutical industry
Official website ↗International / globalRoche
Pharmaceuticals & diagnostics
Official website ↗No matching organizations. Try another name or choose All organizations.
International organizations may also operate in India. “International” does not imply an overseas job offer. Directory reviewed: 26 October 2026.
Student feedback
Learning experiences at MEDICODE
Reviews across our career-focused training programs.
Ananya Sharma
Pharmacovigilance
★★★★★
Course curriculum bahut well-structured hai. Signal detection aur ICSR processing ke concepts practical cases ke sath clear ho gaye.
Rahul Verma
Medical Coding
★★★★★
ICD-10-CM aur CPT coding rules ko bohot simple tarike se samjhaya gaya. Exercises se confidence kafi increase hua.
Priya Patel
Clinical Data Management
★★★★★
eCRF designing aur Data Validation Rules par hands-on learning kafi helpful thi. Industry-relevant training mili.
Aman Gupta
Pharmacovigilance
★★★★★
MedDRA coding aur Aggregate Reporting par detailed sessions the. Mentors hamesha doubts solve karne ke liye ready rehte hain.
Neha Joshi
Medical Writing
★★★★★
Clinical Study Reports (CSR) aur protocol writing ke guidelines ko bohot achhe se cover kiya gaya.
Vikas Rao
Regulatory Affairs
★★★★★
USFDA aur EMA submission processes ke workflows clear ho gaye. Regulatory guidelines ka practical approach accha laga.
Sanya Kapoor
Clinical SAS
★★★★★
Base SAS aur CDISC standards (SDTM/ADaM) par practical exposure mila. Programming concepts crystal clear hain.
Rohan Singh
Medical Scribing
★★★★★
Medical terminology, chart summaries aur live scribing mock sessions se speed aur accuracy dono improve hui.
Pooja Mishra
Pharmacovigilance
★★★★★
Safety Data Sheets aur ADR reporting flow chart ko bohot achhe se explain kiya gaya. Beginner ke liye perfect course hai.
Aditya Saxena
Medical Coding
★★★★★
Modifiers aur HCPCS Level II coding ki practice best thi. Mock assessments se concepts solidify ho gaye.
Deepika Nair
Clinical Data Management
★★★★★
Disquery management aur SAE reconciliation ke practical scenarios ne interview ke liye prepare kar diya.
Karan Malhotra
Pharmacovigilance
★★★★★
Argus Safety database ka overview aur case processing steps bohot acche se samjhaye gaye.
Sneha Kulkarni
Medical Coding
★★★★★
Anatomy aur physiology ke basic revision ke baad coding rules samajhna aur bhi asan ho gaya.
Abhishek Dubey
Clinical SAS
★★★★★
Macros aur Proc SQL ki classes kafi detailed thi. Real-time clinical trial datasets par kaam karne ka moka mila.
Divya Tiwari
Medical Scribing
★★★★★
SOAP notes formatting aur EHR navigation ki training bohot professional thi.
Manish Kumar
Regulatory Affairs
★★★★★
eCTD submissions aur DMF filing ke baare mein jo detail mili, woh pharma industry ke liye invaluable hai.
Megha Rathi
Pharmacovigilance
★★★★★
CIOMS forms aur Line Listings banane ka tarika ab bilkul clear hai. Best coaching experience.
Tarun Bansal
Medical Coding
★★★★★
Inpatient vs Outpatient coding ka difference ab achhe se samajh aa gaya hai. Excellent faculty.
Kritika Sen
Clinical Data Management
★★★★★
Clinical data flow aur Medical coding integration ka concept pehli baar itna clear hua.
Siddharth Jain
Medical Writing
★★★★★
Manuscript drafting aur journal submission guidelines par practical tips kafi kaam aayi.
Poonam Yadav
Pharmacovigilance
★★★★★
Valid vs Invalid cases identify karna aur follow-up process seekhna sabse accha laga.
Akash Chawla
Medical Coding
★★★★★
Surgical and E/M coding sections par extra focus diya gaya jo ki placement ke liye bohot zaroori tha.
Ritu Sharma
Clinical SAS
★★★★★
CDISC SDTM implementation guidelines ko step-by-step explain kiya gaya.
Nikhil Agarwal
Medical Scribing
★★★★★
Physician dictation listening practice se listening aur typing speed dono fast ho gayi.
Swati Deshmukh
Regulatory Affairs
★★★★★
ICH guidelines aur GMP standards par comprehensive notes mile jo revision mein help karte hain.
Mohit Goyal
Pharmacovigilance
★★★★★
Serious Adverse Event (SAE) processing aur expedited reporting timelines clear ho gayi.
Payal Roy
Medical Coding
★★★★★
CPC exam pattern par based mock tests ne exam fear bilkul khatam kar diya.
Vipin Chauhan
Clinical Data Management
★★★★★
Edit check programming logic aur discrepancy management ka practical exposure mila.
Shreya Ghosh
Medical Writing
★★★★★
Patient narratives aur ICSR summary writing ke templates bohot useful hain.
Harsh Vardhan
Clinical SAS
★★★★★
SAS programming step-by-step sikhayi gayi, non-coding background wale students ke liye bhi easy hai.
Rachna Pillai
Pharmacovigilance
★★★★★
Causality assessment aur WHO-UMC scale ki working deeply samajh aayi.
Amitabh Bose
Medical Coding
★★★★★
Cardiology aur Oncology specialities ki coding masterclass bohot insightful thi.
Jyoti Maurya
Clinical Data Management
★★★★★
Database lock aur reconciliation process ki complete training mili.
Sandeep Kumar
Medical Scribing
★★★★★
Anatomy terminology aur pharmacology drugs ke names ab easily samajh aate hain.
Preeti Sinha
Regulatory Affairs
★★★★★
NDA, ANDA aur IND submission lifecycle ka complete overview mila.
Alok Mishra
Pharmacovigilance
★★★★★
Periodic Safety Update Reports (PSUR) ke preparation steps bohot achhe se clear hue.
Tanvi Mahajan
Medical Coding
★★★★★
Coding guidelines ki books (ICD-10, CPT, HCPCS) ko efficiently navigate karna sikh liya.
Gaurav Soni
Clinical SAS
★★★★★
Listing, Tables, and Figures (LTFs) generation clinical trials ke perspective se bohot achhi sikhayi.
Komal Thakur
Medical Writing
★★★★★
Regulatory medical writing vs educational writing ka difference clear ho gaya.
Deepak Sharma
Pharmacovigilance
★★★★★
Quality control (QC) check process aur error prevention techniques par bohot zor diya gaya.
Nisha Khandelwal
Medical Coding
★★★★★
Dermatology aur Orthopedics coding session kafi informative the.
Rajesh Kumar
Clinical Data Management
★★★★★
RAVE EDC system ka practical training session industry standard ke mutabiq tha.
Bhavna Menon
Medical Scribing
★★★★★
Real-time doctor patient conversation sunkar notes banane ki practice best thi.
Sameer Khan
Regulatory Affairs
★★★★★
Post-approval changes aur variation filings ke rules crystal clear ho gaye.
Sonam Kapoor
Pharmacovigilance
★★★★★
Spontaneous reporting systems aur global regulations ki thorough knowledge mili.
Pankaj Verma
Clinical SAS
★★★★★
Data cleaning, merging aur sorting operations ke liye SAS code optimization sikhne ko mila.
Ritika Sen
Medical Coding
★★★★★
Radiology aur Pathology billing guidelines bohot asan tarike se samjhayi gayi.
Vinay Prasad
Clinical Data Management
★★★★★
Medical data coding with MedDRA and WHO-DD efficiently practice kiya gaya.
Meenakshi Iyer
Medical Writing
★★★★★
Abstract writing aur poster presentations ke liye formatting guidelines achhi lagi.
Ashish Gupta
Pharmacovigilance
★★★★★
Pharmacovigilance audit aur inspection readiness par special guidance mili.
Pooja Rani
Medical Coding
★★★★★
CPT modifiers (25, 59, 51) ka use ab bilkul confusion create nahi karta.
Vikramaditya Rao
Clinical SAS
★★★★★
ADaM datasets creation aur traceability mapping ke concepts bohot strong ho gaye.
Shweta Tiwari
Medical Scribing
★★★★★
Patient history, review of systems (ROS), aur physical examination drafting practice badhiya rahi.
Naveen Kumar
Regulatory Affairs
★★★★★
Medical device regulations aur 510(k) clearance process ki details kafi helpful thi.
Garima Sharma
Pharmacovigilance
★★★★★
Duplicate search aur case validation methods industry standards ke according sikhaye gaye.
Sanjay Mehta
Clinical Data Management
★★★★★
Protocol deviation tracking aur query resolution workflow deeply clear hua.
Kavita Nair
Medical Coding
★★★★★
Obstetrics and Gynecology coding chapters bohot achhe se cover kiye gaye.
Rajat Singhal
Clinical SAS
★★★★★
SAS base certification questions and practical coding session badiya the.
Monika Joshi
Medical Writing
★★★★★
Informed Consent Form (ICF) drafting aur ethical guidelines par training great thi.
Yogesh Patel
Pharmacovigilance
★★★★★
Risk Management Plans (RMP) aur benefit-risk balance analysis samajh aaya.
Richa Aggarwal
Medical Coding
★★★★★
Neoplasms aur Endocrinology coding ke tricky questions solve karne ki trick mil gayi.
Mahesh Kumar
Clinical Data Management
★★★★★
Clinical data management lifecycle ka har ek phase detail mein cover kiya gaya.
Simran Kaur
Medical Scribing
★★★★★
Chart documentation speed improve karne ke liye shorthand shortcuts sikhaye.
Bharat Bhushan
Regulatory Affairs
★★★★★
Global submission pathways (ROW countries) ke regulatory requirements clear hue.
Pallavi Deshmukh
Pharmacovigilance
★★★★★
ICSR narrative writing ki templates aur style guide kafi helpful rahi.
Ankit Saxena
Clinical SAS
★★★★★
SDTM mapping specifications read karne aur implement karne ka confidence aaya.
Prachi Gupta
Medical Coding
★★★★★
Neurology and Psychiatry coding rules ko bohot simple examples ke sath samjhaya.
Dheeraj Sharma
Clinical Data Management
★★★★★
Safety data reconciliation process aur discrepancy management clear ho gaya.
Neelam Verma
Medical Writing
★★★★★
Clinical Evaluation Reports (CER) for medical devices ki training bohot unique thi.
Sandeep Chauhan
Pharmacovigilance
★★★★★
Literature screening aur ICSR intake process par hands-on learning mili.
Priyanka Sen
Medical Coding
★★★★★
Integumentary and Respiratory system coding chapters bohot clearly explain hue.
Manish Dubey
Clinical SAS
★★★★★
Macro programming aur advanced data reporting techniques par focus achha tha.
Komal Sharma
Medical Scribing
★★★★★
Emergency room scribing scenarios aur template filling ki practice zabardast thi.
Alok Ranjan
Regulatory Affairs
★★★★★
Pharmacovigilance system master file (PSMF) aur compliance metrics samajh aaye.
Swati Verma
Pharmacovigilance
★★★★★
MedDRA hierarchy (PT, HLT, HLGT, SOC) ko samajhne ka tarika bohot easy tha.
Rahul Mishra
Clinical Data Management
★★★★★
Medical coding dictionaries (MedDRA & WHODD) ki mapping practice badhiya thi.
Neha Patel
Medical Coding
★★★★★
Gastroenterology and Urology coding rules ab easily apply kar leti hoon.
Vikas Kumar
Clinical SAS
★★★★★
Dataset merging (merge, join) ke concepts clear karne ke liye practical examples mile.
Divya Sharma
Medical Writing
★★★★★
Plain language summaries aur patient-facing documents writing ke tips useful the.
Karan Singh
Pharmacovigilance
★★★★★
Signal management validation aur prioritization workflow deep level par clear hua.
Pooja Gupta
Medical Coding
★★★★★
HCPCS Level II codes aur permanent vs temporary codes ka difference clear hua.
Amit Kumar
Clinical Data Management
★★★★★
Clinical database design aur Edit Check specifications likhna sikh liya.
Sneha Roy
Medical Scribing
★★★★★
Cardiology and General Practice chart notes ki practice bohot achhi rahi.
Rohit Malhotra
Regulatory Affairs
★★★★★
Orphan drug designation aur fast-track approval process ki details mili.
Ananya Mukherjee
Pharmacovigilance
★★★★★
SUSAR expedited reporting timelines (7-day and 15-day rules) clear ho gayi.
Mohit Sharma
Clinical SAS
★★★★★
Clinical trial safety tables aur adverse event listings generate karna sikh gaye.
Ritu Kumari
Medical Coding
★★★★★
Mock interviews aur resume building sessions ne placement process asan kar diya.
Siddharth Rao
Clinical Data Management
★★★★★
Data management plan (DMP) creation aur implementation steps clear hue.
Megha Gupta
Medical Writing
★★★★★
Clinical study protocol development aur objective framing ke rules achhe lage.
Abhishek Verma
Pharmacovigilance
★★★★★
Argus database case entry workflow par live demonstration kafi helpful thi.
Tanvi Sharma
Medical Coding
★★★★★
Infectious diseases aur parasitic conditions ki coding exercise kafi thorough thi.
Gaurav Kumar
Clinical SAS
★★★★★
SAS programming fundamentals se lekar advanced clinical reports tak sab cover hua.
Kritika Joshi
Medical Scribing
★★★★★
Medical terminology aur abbreviation shortcuts ne scribing efficiency badha di.
Manish Sharma
Regulatory Affairs
★★★★★
Clinical trial applications (CTA) aur ethics committee submissions ki process clear hui.
Poonam Mishra
Pharmacovigilance
★★★★★
Adverse drug reaction (ADR) seriousness criteria ko identify karne ke rules achhe the.
Akash Verma
Clinical Data Management
★★★★★
Discrepancy management aur query generation life cycle bohot achhe se samjhaya.
Swati Sharma
Medical Coding
★★★★★
Radiology aur Laboratory reporting codes ki coding practice sabse best thi.
Tarun Kumar
Clinical SAS
★★★★★
CDISC standards aur SDTM domain mapping ka practical training session superb tha.
Neha Singh
Medical Writing
★★★★★
Clinical trial safety narrative writing templates aur writing style guide badiya thi.
Vipin Sharma
Pharmacovigilance
★★★★★
Global pharmacovigilance regulations (US FDA, EMA, CDSCO) ka comparative study clear hua.
100 reviews
Frequently Asked Questions
Everything students usually ask before enrolling.
Yes. Major career tracks are structured to include the foundation needed to begin without requiring unrelated courses.
Duration is shown in classes. One core class is planned as approximately 2 instructor-led hours.
Software exposure depends on the course, licensing and training environment. It may be hands-on/simulated, workflow demonstration or industry awareness.
Career support may include resume/ATS guidance, LinkedIn optimization, mock interviews, role-based questions and job-search support. Employment is not guaranteed.
Use the enquiry form below or contact the admissions team directly. Fees can be configured course-wise without displaying them publicly.
Admissions & Counselling
Tell us which career path you are exploring.
Share your qualification and preferred track. The form will open a pre-filled WhatsApp message to the MEDICODE admissions number.