Regulatory Affairs Consultant
Pharmaceuticals - Los Angeles, California, United States
Regulatory Affairs Consultant Employees
Regulatory Affairs Consultant Details
I provide regulatory strategic advice for investigational drug development from early stage (IND enabling) through to NDA filings. I also provide medical and technical writing for clinical, nonclinical, and CMC sections of applications and other correspondences with the FDA.List of services:- IND, ANDA and NDA/BLA administrative information- Clinical summaries (2.5, 2.7) and Clinical Study Reports- Nonclinical summaries (2.4, 2.6)- Quality Overall Summary (2.3)- Expedited programs (Fast Track, Breakthrough Therapy, RMAT, and Priority Review designations)- Pediatric programs (Pediatric Study Plan, Paediatric Investigation Plan)- Rare disease programs (Orphan designation)- Drug Master File annual report- IND Annual Report/Development Safety Update Report- FDA meeting requests- Safety reports- Labelling (package insert/SPL, container labels)- Proprietary names- Gap analyses- Regulatory intelligenceFor inquiries, please send an email to robert.cormack@outlook.com.
