"The RSC Consultant went above and beyond client expectations numerous times to help provide a solution or to suggest enhancements that would streamline processes." Regulatory Affairs Consultant, Pharmalink Consulting
Pharmaceuticals
The Pharmaceutical industry is a knowledge based business, and that means one of its most important resources is skilled, knowledgeable people. Our team at RegSource Consulting is dedicated to providing you the skilled people you require to support all of your regulatory needs. The services we provide to the Pharmaceutical industry include Regulatory Strategy, Regulatory Operations, Clinical, Nonclinical and CMC, Compliance and Regulatory Project/Program Management. These services include:
Strategy for Agency Meetings
GLP/GCP/GMP implementation strategies
Developing Target Product Profiles
Developing Clinical Development Plans
Nonclinical Development Strategies
Chemistry and Manufacturing Strategies
Responses to Agency Questions
Submission Management
Electronic Submission Publishing and Management
Regulatory Operations
Clinical Trial Design and Trial implementation Planning
Review of Clinical Sections of submissions
Provide ongoing regulatory oversight of clinical trials
Provide support in submission of regulatory documentation required for national and international Ethic Committees/IRB
Preparation of Pharmacology and Toxicology sections for regulatory submissions
Pharmacology and Toxicology program review and development
Gap Assessment of current Nonclinical programs
Gap Analysis of all current CMC processes
Preparation and review of all CMC sections for regulatory submission
Assistance in validation activities
Advertising and Promotional Compliance
Labeling and Packaging Compliance
Regulatory Agency Inspection Preparation
GLP/GCP/GMP Audits
Regulatory Program Product Management
Regulatory Product Project Management
Managing current federal and state regulations to ensure your pharmaceutical product is compliant with existing agency requirements within your Clinical, Manufacturing, Nonclinical (Pre-Clinical), Regulatory and Commercial departments is a critical, complex and challenging process.
Our experienced team strives to understand your current corporate timelines and challenges within your organization, and then subsequently matches your requirements with the skilled personnel necessary to achieve your product development goals.
We have access to experienced senior consultants with experience in developing products from proof of concept to commercialization and post marketing.
Contact us and find out how RegSource Consulting can help you find the ideal consultant today.