Product Development
Collaboration offers
Information
We have an in-depth understanding of local and overseas regulations and standards applicable to the manufacturing of both medicines and medical devices.
Starting with the end in mind, our services cover the full product lifecycle and we are well-suited to facilitate and support risk-based product development. Our quality-minded consultants can either share advice, guide you through this process, or deliver hands-on support in any stage of development.
Services you might be interested in:
- GxP & ISO Audits
- Gap analyses
- Quality & Change management
- Supplier selection & Vendor Management
- Implementation of regulatory updates
