QUALITY ASSURANCE = SURPASSED EXPECTATIONS
Among the most important improvements at Accupac are those within Quality Assurance (QA). New Accupac team members are taking it to the next level for our customers—the world’s largest pharmaceutical companies— through:
- A FDA and cGMP regulated environment
- Our QA presence, which follows your project from inception to completion
Accupac is compliant with FDA regulations for drug products and medical devices (21 CFR 211 & 21 CFR 820), as well as Annex V and ISO 13485. We also adhere to customer corporate quality requirements.
Our team includes chemists, microbiologists, lab technicians, QC inspectors, project engineers, validation technicians and regulatory compliance specialists. Working within a cGMP environment and ensuring FDA guidelines are met, they clarify requirements, secure specifications and take pride in exceeding your expectations.
That is how Accupac is becoming the new leader in liquid contract manufacturing.
Click here to contact us to find out how Accupac can surpass your expectations.
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