Alpha-Pharma has a commitment to mankind, a commitment of improving the quality of life for each and every individual through which we constantly strive to innovate, improve and increase the availability of cost-efficient generic medicines to the global market.We believe that medicine should be available to all people regardless of their location, and affordable for them at any income level such that the cost of medical treatment should not be a concern for any part of the population.
Through our commitment we have chosen to focus our resources on generic medicines in which field we aim to increase the availability of our quality medicines and increase global awareness of the vast financial savings offered to society by making generic medicines available to the general population.
Our products can be authenticated through our two factor authentication system at www.Check-Alpha.com
Each product has a serial number which is visible and a security code which needs to be scratched. Both the serial number and the security code needs to be entered on the authentication site to authenticate the authenticity of a product.
Any product that does not authenticate through our system is a counterfeit and must be destroyed or returned to the pharmacy or distributor.
We strongly discourage anyone from purchasing our products as loose ampoules/trays or blisters/strips without cartons. All genuine Alpha-Pharma products are always supplied in a tamper proof carton with intact silver scratch field.
Alpha-Pharma offers in-licensing development of generic pharmaceuticals in our R&D Center as well as outsourcing of full size commercial batch production.
We are able to assist our partners with assignments such as :
- Analytical method development and validation
- Process validation
- Fixed dose formulation development
- Assay & dissolution testing
- Lab scale trial batch production
- Dossier development
- Contract manufacturing on commercial basis
In addition our regulatory affairs team is able to compile technical data as per country specific dossiers and may assist in carrying out bioequivalence studies through relevant clinical research organizations as per required guidelines. Further, we have the capability of manufacturing final dosage forms in country specific cGMP approved facilities.