Find a Consultant

At RegSource Consulting we understand what a time consuming and difficult process it is to find the right individuals to fill your consulting needs. We work closely with our clients to understand their company values and culture, in addition to the specific requirements they need to fill a position.

Please fill out the Consultants skills requirements form below and our Automated Tracking System will locate a Consultant that best matches your requirements. A Client Services Manager will then contact you at no obligation, to discuss your key requirements and help you find the right Consultant.

Level I – Average Understanding of Area         Level II – Good Understanding of Area         Level III – Advanced Understanding of Area
Regulatory Consultant Skill Required In The Following Categories Level 1 Level II Level III
Biotechnology Industry
Pharmaceuticals Industry
Generics Industry
Medical Devices Industry
Over The Counter (OTC) Industry
New Product Application Filings
Generic Application Submissions
Follow on Biologics (Biosimilars)
IND Filings
Orphan Drug Submissions
Clinical Trial Applications
CTD Filings
CTD Module 1
CTD Module 2
CTD Module 3
CTD Module 4
eCTD Submissions
United States Agency Filings
Canadian Agency Filings
European Agency Filings
Latin American Agency Filings
Asia Pacific Filings
Japanese Market Filings
ROW Filing Experience
510K , PMA filings
European Procedures "CE" marking
Scientific Advice
Centralized Procedure
De-Centralized Procedure
Regulatory Consultant Skill Required In The Following Categories Level 1 Level II Level III
Mutual Recognition Procedure
National Procedures
CMC Regulatory Expertise
Clinical Regulatory Expertise
Nonclinical Regulatory Expertise
GMP Audits
GCP Audits
GLP Audits
Labeling Experience
Package inserts/leaflets
SPL (Structured Product Labeling)
US Post Marketing Manufacturing Procedures
Clinical Inspections Preparations
Compliance Gap Assessments
Pre-Approval Inspections
Manufacturing Inspections Preparations
Toxicology & Pharmacology
Gene Therapy
Cell Therapy
Creating Clinical Development Plans
Clinical Study Reports
Combination Products
US and EU Drug Master Files
Device Master Files
Vaccine Antigen Master File (VAMF)
Medical Writing
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  Position   *Company
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  Country   *Phone Number:
*Email Address:     Best Time to Contact you:
  Contract Start Date     Contract length
  Industry     Please Click the Browse button   to upload position description
  Please describe the position   you are looking to fill within   your company     Specific Keyword Requirements   for this Position