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At Orbit pharmaceuticals, we understand the critical importance of maintaining compliance with industry standards and regulatory requirements.

Our pharmaceutical auditing services ensure that your operations meet Good Manufacturing Practice (GMP), Good Distribution Practice (GDP), Good Laboratory Practice (GLP), and Good Clinical Practice (GCP) guidelines, giving you confidence in your processes and product quality.

Our Auditing Services

GMP, GDP, GLP, and GCP Audits

Ensuring compliance with global regulatory requirements, helping you maintain operational excellence.

Vendor and Supplier Qualification Audits

Evaluating and qualifying your suppliers to ensure they meet quality and compliance standards, reducing risks in your supply chain.

Data Integrity Assessments

Conducting thorough reviews to ensure the accuracy, consistency, and reliability of your data in compliance with regulatory expectations.

Mock Regulatory Inspections & Gap Analysis

Identifying potential compliance gaps and preparing your organization for real regulatory inspections to mitigate risks.

Get in Touch

Get in touch to Report Adverse Drug Reactions (ADRs). At Orbit Pharmaceuticals, the well-being of patients is of the utmost importance. Should you encounter any unanticipated side effects or adverse responses linked to our products, we urge you to get in touch with us promptly. Your insights play a pivotal role in upholding the enduring safety and excellence of our medicinal products. To contact our specialist team for ADR reporting please complete the following:

Medical Information Direct Line

+44 (0) 203 096 2886

Medical Information E-mail

[email protected]