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Box 603 , Stockholm, 101 32, SE
Recipharm is a leading contract development and manufacturing organization (CDMO) employing over 5,200 employees. Recipharm provides manufacturing services of pharmaceuticals in various dosage forms, including, sterile fill and finish, oral solid dosage, and biologics; clinical trial material development and manufacturing services; and, pharmaceutical product development. Its biologics segment, ReciBioPharm, works with customers to develop and commercialize advanced therapy medicinal products (ATMPs): pre-clinical to clinical and commercial development and manufacture for new biological modalities. The company operates development and manufacturing facilities in France, Germany, India, Israel, Italy, Portugal, Spain, Sweden and the US.
Recipharm’s technology transfer and manufacturing services helped Arcturus meet its supply needs for its Phase III trial by lyophilizing ARCT-154.
Released By Recipharm
A case study on how Recipharm developed a suitable analysis method for Lobsor Pharmaceutical's advanced Parkinson’s disease treatment, Lecigon® intestinal gel.
We explore the challenges and pitfalls in developing new genetic vaccines, and in manufacturing them following approval.
There is no way to eliminate the risk of failure. However, there are ways to reduce these risks. Learn more in this whitepaper from Recipharm.
Aim to reduce supply chain, compliance, and regulatory challenges during product development.
By: Charlie Sternberg
Provides ReciBioPharm’s customers with access to NewBiologix’s Xcell-Eng-HEK293 cell lines to develop and manufacture AAV Therapeutics.
By: Rachel Klemovitch
Introduces new modular sterile filling system at its facility in Wasserburg, Germany.
Aims to enhance RNA production technologies with the goal of a continuous manufacturing platform and advancement of PAT.
By: Kristin Brooks
Darren Verlenden brings 20+ years of knowledge and expertise to the company through his extensive experience in the Life Science manufacturing sector.
Invests in oral solid dosage, sterile fill & finish and enhances existing development capabilities.
Will scale up protein manufacturing capabilities.
Aim to enganxe sterile manufacturing capabilities in the United States.
Enhances efficiency and speed for customers and patients with three new GMP Pilot Scale suites.
Will create a unique solution for innovators in the gene editing field.
Delivers efficiency and reliability to the pharmaceutical industry by streamlining the product development cycle.
He talks to us about key developments in the inhalation industry and how the formation of a leading global CDMO can provide support in navigating these changes.
Released By Bespak
Spin-out unites 3 sites to create a global CDMO as further significant investments are announced at Holmes Chapel site.
Appoints Dr. Fernanda Masri as Chief Commercial and Innovation Officer and Dr. Christel Fenge as Techno-Commercial Adviser.
Will develop nasally-delivered drug products using proprietary soft mist technology.
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