[vc_row type=”container”][vc_column][vc_custom_heading source=”post_title” google_fonts=”font_family:Open%20Sans%3A300%2C300italic%2Cregular%2Citalic%2C600%2C600italic%2C700%2C700italic%2C800%2C800italic|font_style:600%20bold%20regular%3A600%3Anormal”][vc_column_text]

Excellence in determining excellence

As the Pharmaceutical, Biopharmaceutical and Medical Device Industries add new technologies to the marketplace, it is vital that calibration programs are integral to the method development and validation testing used to ensure regulatory compliance and to ensure that the finished products be of the highest caliber.

Regulators take particular care to make certain that the methods and processes used in the industry are reproducible and validated to assure safety and consistency.

Protocol development and validation testing

Recognizing the critical requirement established by Good Manufacturing Practices as it applies to validations of these programs, Gibraltar provides clients with protocol development and validation testing for both microbiological and chemical validations.

These programs, performed according to the requirements outlined in 21 CFR, include:

  • Cleaning Validation
  • Process Validation
  • Method Development
  • Method Validation
  • Stability Indication
  • Method Transfer

Other key capabilities – We travel to your facility

Gibraltar also serves clients in the area of calibration, assuring that their production flow is not compromised by issues concerning their production environment and equipment. We provide:

  • Clean Room Air Quality
  • Thermal Mapping of Refrigerators, Autoclaves, Freezers, Incubators, etc.
  • On-site Technical Service and Calibration

Recognizing these critical needs of the industry, Gibraltar stands ready to assist your company in developing the assurance needed for your systems.

Contact us today!

To learn more, please call us at (973) 227-6882 or submit a contact form by clicking here.[/vc_column_text][/vc_column][/vc_row]