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Apollo ARI APGDCR-1 Year Course in Clinical Research & Drug Research

Gain in-depth knowledge and practical exposure in clinical research and drug development stages. Kickstart your career in the pharmaceutical industry with our comprehensive course.

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Apollo ARI APGDCR-1 Year Course in Clinical Research & Drug Research

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  1. Apollo Research & Innovations (ARI) APGDCR- 1 Year CourseAdvanced Post Graduate Diploma in Clinical Research

  2. Drug Research Introduction Types of drug innovation : • New molecules (First in class)- New targets through disease pathways analysis • Creates better medicines, explore new indications and make companie market leader • Costly affair, very time consuming and success rate is less • E.g. Drugs for Orphan diseases, Repatha/Praluent (alirocumab) Proproteinconvertasesubtilisin/kexin type 9 (PCSK9) - >USD1 bn revenue • NCE’s extensions for existing/known target- • Simvastatin (Atorvastatin) • New Formulations- Paclitaxel (Taxol)=>Abraxane (nab-paclitaxel) • Copy/Generics- Atorvastatin (Lipitor)

  3. Drug & Clinical Research Drug development stages and activities by stage Large Scale manufacturing Phase IV Drug Discovery FDA Review Pre - Clinical Clinical Trials Phase I 20-100 Volunteers Phase III 1000-5000 Volunteers IND submitted NDA submitted 1 FDA approved Drug 10000 compounds 250 Compounds 5 Compounds Phase II 100-500 Volunteers 5 Years 1.5 Years 6 Years 2 Years 2 Years

  4. Course Module First six months class room training and next 6 months internship • Live trial exposure • Interactions with experts • Infrastructure • Highly skilled personnel • Corporate level training • Interactive sessions • Power point presentation • Real time • On site exposure to clients • Apollo brand • Interview Q&A sessions • Campus placements • Commencement Date: 17th September 2018 • Qualifications- • B.Pharmacy, M.Pharmacy (all branches), Pharm D • B.Sc (Life sciences), M. Sc Biochemistry, Microbiology and Biotechnology • MBBS, BDS, B.P.T, M.P.T, BMMS, BAMS • B.Sc, M.Sc Nursing, B.Tech, M.Tech (Biotech), MS (Pharmaceutical sciences), Pharma M.B.A

  5. Course Contents

  6. Practical Exposure • GCP work shop • CRA feasibility • Site selection visit • Budgeting • Clinical trial agreement review • Site initiation visit • IP receipt and drug accountability • ICF process documentation • Source documentation • Randomization procedures • Paper CRF and eCRF entries, discrepancy resolution • Lab samples handling and processing including PK samples • SAE at site reporting to sponsor and EC • SAE narrative writing • AE/SAE capturing in source notes • CIOMS reporting to EC • Site close out visit • Archival • EC meetings

  7. Courses& Contacts Hyderabad - Ms. Chandana Pal | +91- 9490464322 | +91 9553988504 E-mail : crcourse.hyderabad@apolloari.com New Delhi - Ms. Sunita Kumari | +91- 9560054650 | +91 11 26825612 E-mail : crcourse.delhi@apolloari.com Ahmedabad - Mr. Alex Peter | +91- 7698815042 | +91 7698815045 E-mail : crcourse.ahmedabad@apolloari.com Chennai - Mr. Sathyanarayana | +91- 9841744635 E-mail : crcourse.chennai@apolloari.com

  8. Career Our Top Recruiters • Drug Safety Associate • Clinical Trial Assistant • Clinical Research Associate • Clinical Research Coordinator • Safety Data Analyst • Global PV Scientist • Regulatory Affairs Assistant • Drug Safety Specialist

  9. Thank you!

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