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Priyank Srivastava, R.Ph

Priyank Srivastava, R.Ph

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Personal Information
Organization / Workplace
New Delhi Area, India India
Occupation
Regulatory Affairs Specialist: Medical Devices, IVD's, Drugs, API's, Biologicals
Industry
Medical / Health Care / Pharmaceuticals
Website
http://www.acplgroupindia.co.in
About
Having work experience of around Six years in various spheres of Pharmaceutical Profession. Before joining Regulatory Affairs, had opportunity to work as QA & QC Head. This prior experience has helped me to visualize the problem and has proved boon to a great extent in getting solutions, which is the prime requirement for any Regulatory Specialist.  Central Drug Standard Control Organization New Delhi (CDSCO). Medical Devices (extensively with Class II and Class III devices viz. Cardiac Implants, Orthopedic Implants, Grafts, Dental Implants and almost all Notified Devices and for that applying and received more than hundred registrations), Diagnostics Kits (Critical, Semi-critical and .
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Presentations

(15)
See all

Biological Products

10 years ago • 1910 Views

Cosmetics

10 years ago • 2872 Views

Device Registration

10 years ago • 282 Views

Diagnostic Kits

10 years ago • 3025 Views

Drug Registration

10 years ago • 310 Views

Device Registration in India

10 years ago • 438 Views

Diagnostic Kits Registration in India

10 years ago • 781 Views

Drug Registration in India

10 years ago • 1735 Views

FSSAI

10 years ago • 20153 Views

Manufacturing of New Drug by Export NOC

10 years ago • 705 Views

Narcotics Approval

10 years ago • 687 Views

New Drug Approval in India

10 years ago • 5168 Views

Biological Products in India

10 years ago • 1541 Views

BIS LICENCE UNDER FOREIGN MANUFACTURERS CERTIFICATION SCHEME (FMCS)

8 years ago • 342 Views

BIS LICENCE UNDER FOREIGN MANUFACTURERS CERTIFICATION SCHEME (FMCS)

8 years ago • 805 Views

Documents

(2)

Priyank _ Regulatory

10 years ago • 603 Views

ACPL INRTODUCTION

9 years ago • 72 Views
Personal Information
Organization / Workplace
New Delhi Area, India India
Occupation
Regulatory Affairs Specialist: Medical Devices, IVD's, Drugs, API's, Biologicals
Industry
Medical / Health Care / Pharmaceuticals
Website
http://www.acplgroupindia.co.in
About
Having work experience of around Six years in various spheres of Pharmaceutical Profession. Before joining Regulatory Affairs, had opportunity to work as QA & QC Head. This prior experience has helped me to visualize the problem and has proved boon to a great extent in getting solutions, which is the prime requirement for any Regulatory Specialist.  Central Drug Standard Control Organization New Delhi (CDSCO). Medical Devices (extensively with Class II and Class III devices viz. Cardiac Implants, Orthopedic Implants, Grafts, Dental Implants and almost all Notified Devices and for that applying and received more than hundred registrations), Diagnostics Kits (Critical, Semi-critical and .

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