Our skilled and competent Chemistry group uses a wide range of methods to test raw materials, finished products and packaging components in accordance with compendial procedures including but not limited to: USP/NF, BP, Ph. Eur, JP, CP, FCC, ACS, AOAC, AOCS, In-house and client supplied methods. Over the years, Neopharm has successfully developed/validated/transferred in excess of 3,000 HPLC, GC or other chemistry analytical procedures.
We perform analyses on many types of samples including, but not limited to:
- Pharmaceutical, veterinary, cosmetics, antibiotics, enzymes & natural health products
- Finished products, raw materials, container & packaging components, in-process products, utility systems, gel capsule analysis meeting new USP requirements (gel strength)
We can assist you with numerous routine and specialized techniques and provide support for regulatory submissions (i.e. NDA, IND, CTA).
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