CPhI Online is the largest global marketplace in the pharma ingredients industry
About EPP Ltd
EPP is a GLP compliant Contract Research Organisation (CRO)
assisting pharmaceutical companies with pre-clinical environmental sciences
testing. We ensure the smooth and efficient registration of your products by
following OECD guidelines and can provide bespoke testing as required. We
specialise in GLP complaint testing in the areas of:
· Ecotoxicology; aquatic, marine and terrestrial
· Environmental fate
· Fish metabolism studies
· Controlled substances
· Storage stability
· Physico-chemical testing
EPP can additionally support your pharmaceutical registration and QC testing processes by provid...
Products from EPP Ltd
EPP provides aquatic, terrestrial and marine ecotoxicology testing to evaluate the environmental safety of human and animal health products in order to fulfill the requirements for registration. Our biologists draw upon the expertise of our analytical and synthetic chemists to provide a comprehensive service, with full analytical support, specialising in working with difficult substances including insoluble, unstable, volatile molecules and UVCBs.
Ecotoxicology studies support our core sector expertise:
- Registrations for Plant Protection Products and Biocides
- Registrations for Animal Heath Products
- Pharmaceuticals in the Environment
- New Chemical Notifications & REACH
- Offshore Chemicals Notifications Scheme (OCNS)
- Toxicity-Based Discharge-Consents and Direct Toxicity Assessments (DTA)
The established team of EPP environmental fate scientists have extensive experience gained from supporting global clients. We offer the full repertoire of studies across soils, sediments and natural waters, all conducted to GLP, testing human and animal pharmaceuticals.
With our extensive laboratory capabilities, access to large quantities of ground source freshwater and our strong radiochemistry capabilities we can fully support your requirement for large scale fish metabolism studies in accordance with the new residue data requirements for plant protection products under EC No.1107/2009 where a modified OECD 503 frameworkwould be adopted.
Position your company at the heart of the global Pharma industry with a CPhI Online membership
Your products and solutions visible to thousands of visitors within the largest Pharma marketplace
Generate high-quality, engaged leads for your business, all year round
Promote your business as the industry’s thought-leader by hosting your reports, brochures and videos within your profile
Your company’s profile boosted at all participating CPhI events
An easy-to-use platform with a detailed dashboard showing your leads and performance