DRK ensures compliance of your facilities through our partisanship and coaction approach through our globally experienced advisors- scientists, pharmacists, engineers, and IT experts with established experience in the Life Sciences Industry.
Access to global regulatory consultants with a successful track record of getting approvals for EU GMP, MHRA, PIC/S, WHO PQ & USFDA.
– Flexible Approach in assisting our Clients according to their Requirements
– Off-Site Evaluation
- On-Site Mock Audits & Trainings
- Local Presence of Management staff with Real Time Response
- Project Management Services
- Special focus on Confidentiality
- Cost-Effective
- Queries Handling
- Product Dossier Review
