Name
Celine Locas
Educational Degrees
MSc
Education
MSc in Drug Development, Pharmaceutical Sciences, University of Montreal, Qc, Canada  BSc in Biochemistry, University of Quebec at Trois Rivieres, Qc, Canada
Expertise
Drug/Pharmaceutical Development, GLP Study Auditing, Pharmacokinetics/Toxicokinetics, Regulatory Toxicology, Risk Assessment
Specialties
Provides pharmaceutical and biotechnology industry with senior management experience and expertise in regulatory toxicology and drug development. Emphasis is on program development and management, problem resolution, documentation and peer review. The services provided included but are not limited to:
Non clinical toxicology expertise for all project phases with review and/or preparation of strategic plan for preclinical toxicology. Due diligence et evaluation of in -licencing candidate Implementation and follow up of preclinical toxicology program including selection and qualification of CRO, development and implementation of study protocols, follow up of GLP and non GLP animal toxicology studies, review and correction of study reports.   Safety risk assessment Preparation and review/correction of regulatory documents Project management
Experience
Experienced leader in drug development with over 20 years of industry experience. Former director of toxicology for Virochem Pharma/Vertex Pharmaceutical.  Main expertise in regulatory toxicology, with a recognized track record of streamlining process to save time and dollars on drug development programs. Designed and led preclinical toxicology programs for small drugs in various therapeutic categories including antiviral  and anticancer.
Address
Celine Locas Consultation Inc.
Address 2
290 De Lausanne
City
Laval
State
QC
Zip Code
H7M 5R2
Country
Canada
Telephone
514-708-5961