We work closely with our partners to deliver added value to our clients.
AAPC is a pioneer pharmaceutical consulting company in Oman. As the first company in Oman in its field, AAPC relies on professional partners well known in their field of experience to support AAPC in delivering quality task management and completion to client satisfaction.
AREMA is a company specialized in Regulatory Affairs, CMC, quality compliance, business development and marketing for Pharmaceutical and health care industries covering Africa and other countries. AREMA helps you to outsource services (CTD and medical writing, pharmacovigilance, …) and assist you to introduce many countries in the region.
Asphalion is an international Scientific and Regulatory Affairs consultancy, with offices in Barcelona and Munich.
We collaborate with Pharma and Biotech companies facilitating Drug Development and Regulatory Affairs projects for Drugs, Biologics, Biosimilars, ATMPs and Medical Devices.
Our involvement ranges from early development, through to registration and post-commercialization phases.
In Market Access Asia Pacific Ltd. (IMAAP)
IMAAP is a specialist in Asia Pacific regulatory drug products development, clinical & medical affairs, pharmacovigilance, providing pharmaceutical companies with strategic advice and operational supports to get in-market access of their medicines in the most effective and quickest way. IMAAP also provide the regulatory and scientific/medical affairs consultancy to other healthcare categories, such as medical devices, cosmetics, health supplements, or industrial standard products etc.
Quality PharmServ Romania
Quality PharmServ is a company based in Romania, established in 2007, meant to serve the pharmaceutical field. The products and services we are offering are covering a big part of the process through which a company will have a finished drug, staring with the designing of the manufacturing facility, endowing it with machinery and equipment for all manufacturing and research stages, consulting for elaboration of the GMP documentation an validations, continuing with active substances including the corresponding documentation, with specialized software for compilation of the pharmaceutical dossiers in eCTD/ CTD format, with licensing-in offers for finished drugs or with services of Regulatory Affairs, and finishing with developing a new finished drug, business development, and so on.
SIPS is short for Science Forum for intellectual property & industrial services. SIPS was established in Jordan as limited liability incorporated company in 2000 and got it’s name SIPS in 2002 with territorial extension to most of the Middle East and North African countries. . The main activities of SIPS are Pharmaceutical, Chemical & Biotechnology Intellectual Property Rights, Pharmaceutical Market Authorization and Training.
515 Consulting Group provides expert advice and systems integration services to Pharmaceutical, Biotech and Medical Device companies throughout North America. Our advice and integration services include preparing for, selecting, implementing, validating and operating e-Regulatory applications including eCTD and RPS solutions. 515 Consulting can also help you with outsourcing your submissions, electronic or paper (eCTD, CTD, 510K etc.).