Regulatory Affairs
Hays Pharma provides specialised regulatory affairs talent on either a permanent or temporary basis that can be sourced on a global basis.
These professionals can be sourced as individuals or as a full project team and can assist you with a range of regulatory tasks such as clinical trial applications, regulatory submissions, liaison with regulatory authorities, importation & exportation requests, recognition filings, due diligence audits, product classification and national pricing strategy. Typical searches we undertake are for;
Regulatory Affairs Consultants - Pharma, Biotech and Medical Devices Regulatory Affairs Executives Directors and VP's of Regulatory.
Subscribe to:
Post Comments (Atom)
No comments:
Post a Comment