from the Tribune library:
- Triveritas contines to grow – Julian Braidwood on experience, expertise and depth of knowledge
- German office takes off – Roland Ludwig tackles the German regulatory regime
- Regulatory Affairs
- clinical trials
TRIBUNE – issue 01
April 30, 2012 By
Donna Watson
May 26, 2011 By
Triveritas has appointed Donna Watson as a consultant and member of its Quality Assurance team.
Donna has previously worked on GCP and GLP studies in Animal Health Product Development, Charles River Laboratories and has 4 years veterinary research experience in immunology at Moredun Research Institute along with 2 years R&D experience at biopharmaceutical company Celltech (now UCB).
As reported in Animal Pharm.
John Boyle
March 25, 2011 By
Triveritas has appointed John Boyle as a senior scientific consultant.
Our new CMC Part II expert has over 25 years experience in pharmaceutical development, including formulation, analytics and manufacturing.
His work with Vericore, Grampian Pharmaceuticals and Novartis Animal Health has given him significant manufacturing expertise for complex regulatory requirements.
John also has experience for communicating thorough investigations and testing in Detailed and Critical Summaries (DACS) for the EU.
He has established and managed Formulation and Analytical Laboratories with responsibilities for the development of novel Animal Health products.
As reported in Animal Pharm.
Juliet Greenslade – new consultant for Triveritas
February 18, 2011 By
Triveritas has appointed Juliet Greenslade as a senior scientific consultant.
Juliet will be responsible for providing regulatory advice and support on veterinary biologicals to a range of Triveritas’ clients.
As reported in Animal Pharm.
