Laboratory services for the international pharmaceutical industry
Eurofins│PHAST is the flexible laboratory service Provider
for human and veterinary drug products
- Small Molecules
- Biologics/Large Molecules
Analytical Development, Quality Control
- Analytical support (e.g. structure elucidation, drug analysis)
- Drug development services (e.g. method development and validation, stability studies incl. controlled storage)
- Market supply (e.g. batch release testing, batch release by QP, stability studies incl. controlled storage)
- Clinical Trial Supply Management (CTS)
- On-Site Services (Insourcing with Eurofins Professional Scientific Service®)
Reference Standards
- You can find your daily analytical needs of USP Reference Standards in our webshop for professionals, incl. customs clearance/EU import.
- In addition in our webshop for professionals we offer EDQM / Ph.Eur. Reference Standards
- USP training courses on monograph-compliant handling of reference standards can also be found at www.reference-standards.com
The laboratories in Homburg and Constance are GMP-certified. The multiple successful inspections by the U.S. FDA are additional confirmation for the customers of Eurofins | PHAST for permanently highest quality level.
Eurofins | PHAST operates a biological safety level 2 laboratory (BSL 2) .
As a strategic partner, Eurofins│PHAST assumes worldwide responsibility for quality in the development and manufacture of pharmaceuticals - all services: one-stop contact!
Inquiries
Contact: PharmaTesting@eurofins.com
Tel: 0049 / 684 192 420
Reference Standards
Tel: 0049 / 684 192 424 56