At CDG, we understand the critical importance of compliance with EU GMP regulations in the pharmaceutical and healthcare sectors. Our team of highly skilled and experienced professionals is dedicated to helping your organization meet and exceed these standards. With a commitment to excellence, integrity, and accuracy, we strive to be your trusted partner in achieving and maintaining GMP certification.
Comprehensive EU GMP Certification Services:

1. GMP Compliance Audits: Our expert auditors conduct thorough assessments of your manufacturing facilities, quality management systems, and processes to ensure compliance with EU GMP regulations. Through meticulous audits, we identify areas for improvement and provide actionable recommendations to enhance your GMP compliance.
2. Documentation Review and Development: Proper documentation is at the core of GMP compliance. We assist your organization in reviewing and developing comprehensive documentation, including standard operating procedures (SOPs), batch records, and quality manuals, tailored to meet EU GMP requirements.
3. Training Programs: Stay ahead of the curve with our specialized training programs. Our courses cover a wide range of topics, including GMP principles, regulatory updates, and best practices. Empower your team with the knowledge and skills necessary to maintain GMP compliance.
4. Validation Services: Ensure the integrity of your processes and systems through our validation services. We validate equipment, processes, and computerized systems to meet GMP standards, providing you with the confidence that your operations are consistently producing high-quality products.
5. Risk Management and CAPA Support: Proactive risk management is crucial in maintaining GMP compliance. We assist your organization in identifying and mitigating risks, as well as developing effective Corrective and Preventive Action (CAPA) plans to address any deviations from GMP requirements.
6. Regulatory Consulting: Navigating the complex landscape of regulatory requirements can be challenging. Our regulatory experts provide consulting services to guide you through the intricacies of EU GMP regulations, ensuring that your organization remains in compliance.

Why Choose CDG:

• Accreditation and Expertise: CDG is an accredited testing laboratory with a team of experts possessing in-depth knowledge of EU GMP regulations and industry best practices.
• Customized Solutions: We understand that each organization is unique. Our services are tailored to address the specific needs and challenges of your business.
• Timely and Efficient Service: We recognize the importance of time in the pharmaceutical industry. Our team is committed to delivering timely and efficient services without compromising on quality.
• Long-Term Partnership: Beyond certification, we aim to build long-term partnerships with our clients, providing ongoing support to adapt to evolving regulations and industry standards.

Choose CDG as your partner in achieving EU GMP certification and experience the assurance of quality, compliance, and excellence in pharmaceutical and healthcare manufacturing. Contact us today to embark on a journey toward GMP excellence.