PrimaPharma expands Analytical Chemistry Laboratory Capabilities

December 2016 – PrimaPharma, Inc. has acquired state of the art Analytical Chemistry equipment including UPLC and HPLC equipment.  “This instrumentation allows PrimaPharma to provide analytical assay service for pharmaceuticals to improve manufacturing process timing with acceptable methods and costs for our customers” says Dr. Nayaz Ahmed, Director of QC and Analytical Services for PrimaPharma, […]

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On December 30, 2016, posted in: News by

PrimaPharma acquires capability for aseptic filling of syringes.

October 2016 – PrimaPharma, Inc. announces the acquisition of syringe filling equipment to add to its pharmaceutical manufacturing sterile processing capabilities. The syringe filling equipment will give PrimaPharma the capability to aseptically fill syringes from 0.1mL to 10 mL in lot sizes ranging from 2,000 to 3,000 syringes per 8 hour shift.  The equipment IOQ […]

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On October 1, 2016, posted in: News by

PrimaPharma, Inc. Re-certified to ISO 13485:2003.

May 2016 – PrimaPharma, Inc. recertification inspection by the British Standards Institute was successfully completed and a Certificate of Registration was issued.  British Standards Institute issued Certificate of Registration #FM 59723 expiry date of 2/28/19 to PrimaPharma, Inc at the end of the inspection.  “this re-certification by the British Standards Institute exemplifies the PrimaPharma commitment […]

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On May 1, 2016, posted in: News by

Sarah Dziabo named associate Director of Quality Assurance.

January 2016 –  PrimaPharma announced today that Sarah E. Dziabo has been appointed associate Director of PrimaPharma Quality Assurance Department.  Sarah has extensive experience in Q.C. & Q.A. working at Medtronic Cardiopulmonary, Alsius, Micro Quality Labs as well as PrimaPharma, Inc.  Her experience includes document control, quality control, quality assurance, analytical chemistry, microbiology, pharmaceutical and […]

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On January 30, 2016, posted in: News by

PrimaPharma validates High Recovery Vial aseptic process.

January 2016 – PrimaPharma announces that it has successfully validated their aseptic filling process for High Recovery Vials by completion of a rigorous media fill campaign.  High Recovery Vials are a specialty vial with a “V” bottom that allows for a syringe to fully access the contents of the vial with a syringe.  This type […]

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On January 1, 2016, posted in: News by

PrimaPharm to Sponsor 8th Annual Global Pharma Manufacturing Summit 2013

June 26, 2013 – PrimaPharm will be a sponsor and exhibitor at the 8th Annual Global Pharma Manufacturing Summit 2013 taking place June 27th-28th, 2013 at the Westin Copley Place, Boston.  The Global Pharma Manufacturing Summit is a premier networking opportunity for industry leaders involved in small molecule and biologic pharma manufacturing.  At the event, senior […]

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On June 26, 2013, posted in: News by

PrimaPharm successfully completes latest FDA cGMP inspection

June 18, 2013 – Today PrimaPharm has announced the US Food and Drug Administration (FDA) has completed its most recent inspection of the company’s manufacturing facility.  The entire facility and the quality systems used for the manufacture and release of drug products were subject to a detailed compliance inspection.  The inspection found the facility to be compliant with the […]

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On June 18, 2013, posted in: News by

PrimaPharm Announces Successful ISO 13485:2003 Recertification Audit

March 15, 2013 – PrimaPharm, Inc., a contract manufacturer of drugs and medical devices, announces the successful completion of its ISO 13485:2003 recertification audit for its production facility located in San Diego, California.  PrimaPharm has maintained its ISO 13485:2003 certification with the British Standards Institute since 2000, and the recently completed audit recertifies the company through 2016. ISO […]

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On March 15, 2013, posted in: News by