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Contract Service 12 record(s)；
pMDI and DPI CMO
Till now we are the only one can provide and manufacturing MDI drug in Taiwan. Our facility complies with PIC/S GMP and also follows EMA and US FDA GMP standard.
Contract Development and Manufacturing Organization (CDMO)
As a contract development and manufacturing organization (CDMO), Formosa Laboratories (Formosa Labs) offers full-service for both general and high potency API (HPAPI) for all stages of drug development for both clinical trial material (CTM) and commercialized (NDA). Our GMP compliance has been approved by DOH of Taiwan, US FDA, BGV of Germany, EDQM and PMDA of Japan since 2000.Process Research
Contract Manufacturing /Development
Benchmark pharmaceutical manufacturerOrient Pharma's Yunlin Plant was built with the highest standards of manufacturing, packaging and supporting system.The plant passed the GMP inspection by US FDA, the PIC/S GMP inspection by Taiwan FDA, and received “Accreditation Certificate of Foreign Drug Manufacturer” from Labour and Welfare (MHLW) in Japan.The plant is equipped with facility
RD Formulation and Development of Finished Products
We are looking for global partner to do co development from RD status to file in US, EU and the other advanced countries.
OEM Tissue Culture Seedings
Under srict control in each stage of production from choosing the healthy plants, applying cutting edge virus detection technology, establishing production S.O.P. and QC procedure, Tai-Ling is committed to provide the highest quality of phalaenopsis plants for our customers.
CRAM ServicesScinoPharm offers world class services related to the development and manufacturing of clinical, small-scale, and commercial-stage active pharmaceutical ingredients (APIs) and intermediates. Dedicated Contract Research Organization (CRO) and Contract Manufacturing Organization (CMO) are to provide fast response to customers' needs, combined with a flexible, reliable, and competitive
CMC / CDMO (Contract Development and Manufacturing Organization)
Mammalian system- Monoclonal antibodies (novel and biosimilar mAbs)- Fc-fusion proteinsMicrobial system- (Pegylated) Recombinant proteins- Plasmid DNA- Protein vaccine- Biosimilars / BiobettersCell Line Engineering- CHO & E. coli platforms (others such as NS0, PER. C6, HEK 293, hybridoma, pichia)- From DNA construction to protein expression- Highly productive stable cell line- Medium screening
OEM/ODM /CRO/CMO Services
We are a certified enterprise, which has passed the certifications of PIC/S GMP, ISO9001, ISO17025, ISO14001, OHSAS18001 and ISO22000. Therefore, we have very good reputation of manufacturing more than 400 products including therapeutic medicine, health supplement and skin care product. R&D capability is our best strength; several new drug applications have been processed recently. Dosage
Pilot scale up development and cGMP manufacturing of biopharamaceutical drug substance (DS)
Process Development Capacity- Flow sorter for cell pool titer enrichment- Automated photo-documentation for monoclonal formation- Micro bioreactor system for cell line development and process optimization- 2L/5L bench top bioreactors- 2L/20L fermentors- 20L and 100L stainless steel bioreactors- 50L single use bioreactor- Disc centrifuge and continuous centrifuge- Homogenizer and refolding tank- Liquid
With abundant fermentation's experience, Grape King not only provides sufficient raw materials for customers, but also welcomes scale-up microbial fermentation authorization businesses (OEM).Grape King Bio owns a fermentation production capacity of 281 tons. The fermenters size range from 200L, 500L, 40T, to 50T. The diversity of fermenters can satisfy customer specific needs. The fermentation
Process Development Service
JHL has scalable platform technologies for cell culture and purification to provide optimal protein product qualities and yield. We develop processes in 3L and 50L, and then scale it up to 200L, 500L or 2,000L for use in non-clinical, clinical trials and commercial production.Cell Culture Process Development (USP)CCDP develops robust processes suitable for GMP clinical and commercial manufacturing