Broughton is an independent life sciences contract research organization serving a global roster of clients from the UK, Europe, North America, the Middle East, Asia, and Australia. We offer high-quality in-house analytical testing services integrated with scientific consultancy and global regulatory support. Our in-house laboratory testing facilities are GMP compliant and ISO/IEC 17025 accredited. We are regularly inspected by the Medicines and Healthcare products Regulatory Agency (MHRA), the US Food and Drug Administration (FDA), and the United Kingdom Accreditation Service (UKAS).
With over 15 years of scientific experience and a world-leading team of scientific and regulatory consultants, we support our partners in bringing innovative products to market to deliver better health outcomes.
Pharmaceutical Analytical Testing
Meeting Global Regulatory Requirements through Specialist Chemistry, Manufacturing, and Controls (CMC) Analytical Services
Whatever the requirements of your pharmaceutical project, we can help with a full range of GMP testing and analysis services. From early development characterization and formulation analysis to analytical method development, stability studies, extractables and leachable studies, and QC release testing.
Our Pharmaceutical Analytical Testing Services include:
- Analytical Method Development
- Quality Control Release Testing
- Stability Storage and Analysis
- Inhalation Testing Services
- Extractables & Leachables (E&L)
- Product Assessment
Pharmaceutical Consultancy Services
Improving Quality of Life Through Scientific and Regulatory Consultancy
We help clients deliver life-enhancing products to market through analytical testing excellence integrated with best-in-class scientific consultancy and regulatory compliance.
Our Pharmaceutical Consultancy Services include:
- Product Realization
- Analytical Chemistry Consulting
- Toxicology Assessment
- Environmental Assessment
- Regulatory Consultancy
- EU/UK MAA Regulatory Support and Submission Service