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Box 603 , Stockholm, 101 32, SE
Recipharm is a leading Contract Development and Manufacturing Organization (CDMO) employing over 5,000 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 Advanced Bio segment 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
Introduces new modular sterile filling system at its facility in Wasserburg, Germany.
Invests in oral solid dosage, sterile fill & finish and enhances existing development capabilities.
By: Kristin Brooks
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.
Delivers efficiency and reliability to the pharmaceutical industry by streamlining the product development cycle.
Spin-out unites 3 sites to create a global CDMO as further significant investments are announced at Holmes Chapel site.
Will develop nasally-delivered drug products using proprietary soft mist technology.
Aims to achieve greater quality oversight, use resources more effectively, accelerate validation, and maintain inspection readiness.
By: Anthony Vecchione
Recipharm will provide analytical and process development capabilities to support toxicology studies, as well as GLP manufacturing of lipid nanoparticles.
New analytical lab in Bengaluru, India enhances global testing for nitrosamines, extractables and leachables, and elemental impurity testing.
By: Tim Wright
Research using Honeywell’s Solstice Air will be conducted at Recipharm’s inhalation development facility in RTP, NC.
The FDA decision provides Recipharm with a platform on which to build out its manufacturing capabilities for new modalities in the biologics space.
Brings experience in building and developing strong teams in supporting organizations through its next phase of growth.
Stevanato will support the development and production of pre-fillable syringes for use in Recipharm’s soft mist inhalers.
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