UK/IE Qualified Person (QP) Services: Ensuring Compliance and Quality

Our team of experienced QPs provides comprehensive and tailored support to help you navigate the complex UK/IE regulatory landscape and ensure the quality and compliance of your pharmaceutical products.

Our QP Services Include:

Qualified Person Release: Our QPs provide expert release certification to ensure your products comply with the relevant UK/IE regulations, including the Human Medicines Regulations 2012 & EU-GMP requirements.

GMP/GDP Compliance: We provide comprehensive support to ensure your operations comply with the Good Manufacturing Practice (GMP) and Good Distribution Practice (GDP) requirements, including gap analysis, documentation review, and internal audits.

Regulatory Submission Support: Our team provides guidance and support throughout the regulatory submission process, including assisting with the preparation of applications and responding to regulatory agency questions.

Quality System Assessment: Our QPs perform in-depth assessments of your quality systems and processes to identify areas of improvement and ensure regulatory compliance.

Ongoing Regulatory Support: We provide ongoing support and guidance to help you stay compliant and up-to-date with the latest UK/EU regulatory requirements. 

At Innovind Pharma, we are dedicated to providing the highest quality QP services and ensuring the success of your pharmaceutical projects. Contact us today to learn more about how we can help you meet your UK/IE regulatory needs.