6 16

Documentation Vital to Compliance in Contract Manufacturing

Establishing clear expectations about documentation and procedures plays a key role for contract manufacturers and own-label distributors in verifying FDA compliance with current good manufacturing practices (cGMPs) of dietary supplement products.

The increasing reliance on contracted services by both large and small marketing dietary supplement companies has created challenges in understanding and meeting both individual and mutual responsibilities. Working together to understand and meet those responsibilities goes a long way to achieving success for each party in terms of reliability of service, uninterrupted supply of high-quality product, a sustainable and profitable business relationship and avoidance of potential FDA issues.

Register to view the full article

Registering as a member of Natural Products INSIDER will give you free access to premium content including digital magazines, webinars, whitepapers and more.

Hide comments

Comments

  • Allowed HTML tags: <em> <strong> <blockquote> <br> <p>

Plain text

  • No HTML tags allowed.
  • Web page addresses and e-mail addresses turn into links automatically.
  • Lines and paragraphs break automatically.
Publish