Services
Pharma.MT offers a range of services not only aimed at Distribution and Marketing of Pharmaceuticals and other pharmacy based and beauty products, but also covering the licencing and regulatory hurdles involved in registering products for the European Market.
Our Services
Marketing
Storage
Distribution
Regulatory Affairs
EU QP Services
GMP
Marketing
Pharma.MT takes great pride in knowing that they deliver the highest quality of services to their partners and their operating markets. The dynamic team that make up Pharma.MT have decades of experience in marketing pharmaceuticals, biologic’s, dermatological and other healthcare products as well as cosmetics, beauty and primary care items. Our Marketing department consists of sales and medical representatives as well as graphic designers and digital marketing experts, capable of producing all our marketing material and carrying out traditional and digital marketing campaigns.
Storage and Distribution
We have state of the art IT systems and storage facilities spanning more than 600 m². Our warehouses are climate controlled according to GDP and we have an in house cold storage room for refrigerated products. We also offer the possibility of storage in the Freeport. Pharma.MT Ltd has both a significant distribution fleet and a close working relationship with local wholesalers enabling us to provide all our clients with daily deliveries. Through this distribution system we service all pharmacies, health stores and retail outlets in Malta and Gozo as well as centralised government agencies.
Regulatory Affairs
Regulatory services are offered either standalone or alongside pre wholesale logistics services and clinical trial services. Regulatory services can be contractual or ad hoc and are targeted to small and medium pharmaceutical companies and biotechs. Through our ever-expanding network of partnerships we are in an ideal position to bring together pharmaceutical suppliers, regulatory professionals and Competent Authorities in the most effective way
Our full list of regulatory services;
- Qualified Person (QP) services including batch release
- Responsible Person (RP) Services
- Site visits and auditing to ensure compliance with GDP/GCP/GMP
- Wholesale licence applications
- Writing and amendment of SOPs
- Regulatory advice (UK, FDA & EMEA)
- Liason with competent authorities on all aspects of compliance
- Analytical testing
- Pharmacovigilance
Qualified Person Services
Qualified Person Release (QP Release) is available as part Pharma.MT''s Regulatory Services, which complements the company's wider offering to the pharmaceutical industry and healthcare sector. For clients without an EU presence, we have extensive experience of accepting pharmaceuticals and biopharmaceuticals into the EU, conducting QP Release and navigating the EU regulations.
PV / CV
Our Pharmacovigilance/ Cosmetovigilance department is responsible for monitoring and reporting the effectiveness and any adverse effects or side effects of pharmaceutical and cosmetic products we represent. All the data is meticulously recorded, analysed and processed in order to maximise product safety and performance, and minimise adverse effects. Our department also undergoes regular audits by external PV companies to ensure we are constantly up to date with global requirements
GMP
We follow Good Manufacturing Practice to ensure all our products are of the highest quality and all our processes and procedures are controlled in order to minimize any potential risks to the final products we are distributing. GMP is followed in all our processes, including our premises and training of all our staff to maintain highest standards. An in-house Qualified Person (QP) is available to constantly monitor all our processes and also to provide the service of Batch release when required.
