PHARMACEUTICAL CONSULTING , QUALITY ASSURANCE , REGULATORY SUPPORT , QUALITY MANAGEMENT SYSTEMS

Lucid Pharmaceutical Compliance provides end-to-end consulting services for Pharmaceutical, Biopharmaceutical and Agricultural projects. We will ensure that your project is supported from the initiation phase, right through to the operational phase, by providing services that are intelligible, precise and easy to implement.

COMPLIANCE

Lucid Pharmaceutical offers comprehensive consulting services to facilities that require GMP, EU-GMP and GACP regulatory compliance. We accurately adhere to the regulatory guidelines set forth by the South African Health Products Regulatory Authority (SAHPRA), Pharmaceutical Inspection Co-operation Scheme (PIC/S), European Medicines Agency (EMA) and International Organization for Standardization (ISO). We will guide and support you through every step of the licensing process.

MEDICINAL CANNABIS

Lucid Pharmaceutical provides licensing and compliance support to cannabis facilities that have an interest in cultivating (GACP), processing (GMP) and/or manufacturing (GMP) cannabinoid-containing products. We have been successful in obtaining GACP and GMP licensing for cannabis facilities, as per the Medicines and Related Substances Act 1965 (Act 101 of 1965), through the provisions of Section 22A(9)(a)(i) and Section 22C respectively.

PROJECT SUPPORT

We are involved from project conceptualization right through to the validation of the facility. Facility design can be an intimidating process, at Lucid Pharmaceutical we will help you design the perfect facility to meet your project’s operational, quality and regulatory needs. We offer a wide variety of support services, including facility design support, equipment and utility design reviews, process optimization and validation services (DQ,DR,IQ, OQ, PQ,PV,CV) .

Licensing

Quality Assurance

Development

Other Solutions

About us

Innovative. Honest.
Simple.

We stand for honesty, clear communication and innovative working solutions. Our team of highly skilled and knowledgeable experts has a wealth of experience in the quality assurance, quality control, validation, facility design, business development and regulatory compliance disciplines. We specialize in medicinal licensing through the SAHPRA and EMA, by adhering to current Good Manufacturing Practices (cGMP) and Good Agricultural and Collection Practices (GACP).

Contact Us

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