We are updating our Facility 1 to comply with the GxP standards!
Embedding quality into the product – that is what we at Ocimum Life Sciences believe in and work towards, during any of our custom synthesis and semi-bulk scale manufacturing. With an ISO 9001 certification and a culture of continuous quality improvement already in place, we have been delivering the requested products in the highest quality standards to our clients. We are now further upgrading ourselves to knock at the doors of the next milestone!
Material, information, and process flows are being reimagined to prevent cross-contamination further. Stress is being laid on documenting “all” our operations while complying with the ALCOA++ principles. A big shout out to our ERP partner – KeaGMP – owing to which we have been able to push this transition at an unprecedented pace. Visual management and work instruction letters are being strengthened to enable our people to seamlessly perform any equipment handling. All this while ensuring that employee satisfaction, safety, and environmental sustainability are at the heart of all our operations.
What’s next? – Phase 1 of this transition is touted to be completed by July 15th, 2024. We are taking giant strides towards becoming an “anytime audit-ready facility”. If you have any suggestions for us during this journey – please feel free to reach out to us at contact@ocimumls.com or visit our facility. We are eager to partner with you in the journey of improving the quality and duration of human lives!