SA-FORD, A division of Sharon Bio-Medicine Ltd. offers various toxicology services related to animals as per international rules and regulations (OBCD GLP EPA, ICH, ISO 10993).

INTERMEDIATES & ACTIVES Fully equipped Process development Labs & Analytical Labs are managed by highly experienced team of professionals. Their combined expertise in Chemistry, Analytical method development and engineering provide the necessary advantage to complete projects within short time spans. These labs are complimented by Kilo-labs & Commercial-Scale plants which operate as per cGMP.

FINISHED DOSAGE FORMS Sharon 's core competency is development of a range of Tablets and Capsules including modified release products. The laboratory is well equipped with senior scientists to handle technology transfer projects from our esteemed partners and carry out variations to suit our manufacturing equipment The Pilot Plant is ideally designed to carry out scale up & submission batches under cGMP.

REGULATORY AFFAIRS A centralized regulatory affairs department at Sharon , coordinates with the Development Labs & the manufacturing facilities for all product relevant data. They also guide them from time to time to ensure compliance to the applicable guidelines. Their expertise lies in compilation & verification of DMF & Dossiers as per specific country regulatory requirements.