MEDELLIGENT PHARMACEUTICALS LTD
How can we help your business.
Qualified Person (QP) Services and Batch Release
Medelligent Pharmaceuticals Ltd (Medelligent) undertakes the certification and release of batches manufactured in the EU and/or in third countries. Our highly experienced Qualified Persons (QPs) cover non-sterile and sterile Finished Dosage Forms (FDFs) as well as starting materials including Active Pharmaceutical Ingredients (APIs). Access …
Qualified Person (QP) Services and Batch Release
Our staff comes from various disciplines of the pharmaceutical sector including synthetic chemistry and chemical engineering. These qualifications coupled with their QP experience allows Medelligent to carry out effective GMP audits of starting materials, API and FDF manufacturers. We are experienced …
Qualified Person (QP) Services and Batch Release
Our dedicated team has the experience to put in place Quality Management Systems (QMS) for the pharmaceutical industry and to train the customer on site, if requested. We can deliver a tailor-made QMS to satisfy the needs of our clients. Our QMS consulting cover Manufacturing/Import Authorization, Wholesale Distribution Authorization …
Plant Layout Materials and Machinery Selection
We design plant layouts or propose layout modifications of new and existing FDF plants. The layout proposal is based on customer needs and requested capacities. Our commitment is to deliver a cGMP conceptual design of what the customer needs. Materials and machinery are selected from reliable and price competitive suppliers …
Project Management
We can manage customer projects ranging from facility construction to R&D. Facility construction and machine delivery is part of our project management services we offer. Our team has outstanding combined experience in successful delivery of projects. We assist pharmaceutical companies to perform Performance Qualifications (PQ) as well as Factory …
About Medelligent
Medelligent offers consulting services for the pharmaceutical industry. With over 25 years of experience in the field of pharmaceuticals, we specialize in providing our clients with expert opinion, training and services in order to meet the growing demands of Good Manufacturing Practice (GMP) and Regulatory compliance. Our dedicated staff of EU Qualified Persons (QPs) as well as responsible Persons (RP) and experts are ready to support your company’s needs and provide solutions that can be implemented in a professional and timely manner. Our approach to our consulting services relies on knowledge and pharmaceutical technology principles.