Medical Drugs Downloads
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PremiumPoster: Tips and trips for cannabinoid separation
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ReadyCircuit Bags and Tubing Assemblies – Brochure
ReadyCircuit™ assemblies are part of the Cytiva ReadyToProcess™ product platform (Fig 1). ReadyCircuit assemblies allow you to simplify and speed up bioprocessing, thus enabling biopharmaceutical companies, contract manufacturing organizations (CMOs), and biotech start-ups to accelerate product development and reduce costs of initial investments. In addition, single-use ReadyCircuit ...
By Cytiva
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SEFIA S-2000 Cell Processing Instrument - Brochure
The Sefia™ multifunctional instrument is designed for cell therapy product manufacturing. The Sefia Cell Processing System, which is comprised of the instrument, protocol software, and disposable kits, allows you to perform upstream or downstream processing steps in a functionally closed and automated manner. You have the flexibility to customize each step to run only the operations you ...
By Cytiva
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Sepax C-Pro Cell Processing Instrument - Brochure
The Sepax™ C-Pro Cell Processing System is an automated and functionally closed technology for cell processing when developing and manufacturing cell therapy products. The system, which is comprised of the instrument, Sepax C-Pro protocol software, and kits, allows you to combine multiple processing steps in a versatile manner. These steps include but are not limited to enrichment, magnetic ...
By Cytiva
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The New EU GMP Annex 1 Revision 2017 Comments from Industry Experts - Applications Note
The updated EU GMP Annex 1 Draft was released for public comment in December 2017, and the industry experts at Particle Measuring Systems have shared their response on the ...
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Classification, Qualification and Monitoring According to EU GMP Annex 1 Rev 12 - Applications Note
The latest Annex 1 draft has some new definitions and guidance regarding Cleanroom Classification, Qualification, and ...
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Xuri Growth Factors Cell Expansion - Datasheet
Growth factors regulate many aspects of cellular function, including proliferation and differentiation. They are widely used for the expansion of T lymphocytes and other primary cell types in cell therapy and research applications. Xuri™ IL-2, IL-15, and IL-21 growth factors are developed following the recommendations of USP <1043> “ancillary materials for cell, gene, and ...
By Cytiva
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Fast Trak Process Development Services - Brochure
“In 1981, I started my first job in a biomanufacturing company and I have spent the years since then developing processes and building facilities to speed molecules to the clinic and to market faster and with less risk. My early experiences gave me insights into the pains and pressure points when developing a drug and what is needed to succeed. Many of our scientists have a similar ...
By Cytiva
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The New EU GMP Annex 1 Draft: Impact on Environmental Monitoring Programs - Application Note
Introduction On December 20th, after intensive research and debates, the draft for a Revision of ANNEX 1 ("Manufacture of Sterile Medicinal Products") of the EU Guideline for GOOD MANUFACTURING PRACTICE for drug products and drug substances was published for public comment. This updated document will set a milestone for adjustments needed within European agencies overseeing drug products ...
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Compressed Gases: An Important Component of an Environmental Monitoring Program in a Pharmaceutical Manufacturing Environment - Application Note
Quality Attributes of Manufactured Pharmaceutical Products The quality attributes of manufactured pharmaceutical products include the physical, chemical, and microbiological characteristics of the raw materials, excipients, active pharmaceutical ingredient (API) as well as the final drug product (Table 1). Absence of microbiological contamination is considered a critical quality attribute due to ...
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Data Integrity: Understanding and Becoming Compliant with GMP and FDA Requirements - Application Notes
Introduction Data integrity means data (such as from personnel or environmental monitoring) that is accurate, complete and repeatable, which in turn ensures the product's quality and public safety. In recent years, infractions relating to data integrity have been noted in several Food and Drug Administration (FDA) warning letters, but it is not a new concept. The importance of record-keeping in ...
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Xcellerex XDUO Mixer - Datasheet
Xcellerex XDUO Mixer is an intelligent, plug‑and‑play, single‑use mixing system for clinical and commercial production of biopharmaceuticals, vaccines, and other biologics (Fig 1). The system supports upstream and downstream applications for automated mixing of buffer, media, product and intermediates, as well as other process fluids. XDUO features powerful onboard automation ...
By Cytiva
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Encapsulator B-390 - Brochure
The versatile system for controlled encapsulation of active ingredients and materials for laboratory- scale research and development work. The simplicity and adaptability of the device allow its use in a variety of areas – pharmaceuticals, materials, cosmetics, the food industry and ...
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Model B-390 - Encapsulator for Innovative Microbeads and Microcapsules - Brochure
The versatile system for controlled encapsulation of active ingredients and materials for laboratory- scale research and development work. The simplicity and adaptability of the device allow its use in a variety of areas – pharmaceuticals, materials, cosmetics, the food industry and ...
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B-440 - Wet Digester System - Technical Datasheet
Instrument for parallel pre-incineration of samples with automatic acid fume exhaust. The B-440 is used in different industries such as pharmaceutical production, food quality control or environmental testing. Temperature/time profiles can be programmed and stored for optimal process safety, reproducibility and ease of use in routine ...
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Pharmaceutical Industry - Brochure
As a highly specialised engineering and production company ERDWICH offers exceptional services in recycling and shredder technology, backed up by over 30 years of experience. Shredding machinery, special solutions, complete recycling systems and global services are our core competencies, to which our team dedicates itself enthusiastically every day. Owner-managed, with personal, intensive ...
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NIRS XDS MasterLab Analyzer - Brochure
The NIRS XDS MasterLab Analyzer enables manufacturers in the pharmaceuticals industry to quickly analyze solid dosage forms, such as tablets, capsules, caplets, gel tablets, and gel capsules, without destroying the sample. The NIRS XDS MasterLab Analyzer can also be used to analyze solids in vials. The samples are analyzed in either reflection or transmission ...
By Metrohm AG
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SnowPure - Model XL-EXL HTS Series - High-Temperature Pharmaceutical EDI - Datasheet
High Temperature Stable EDI for Pharmaceutical OEMs Now to 85°C. Key Benefits Include: Hot Water Sanitizable at 85°C / 185°F - 15 min up to 2 hrs (see USP recommendations). Rapid Heat/Cool Cycle — up to 160 cycles. New High Temperature FDA Urethane Materials. Pharmaceutical Stainless Steel (EXL option). Light, Compact, Easy to Ship and ...
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Pharmaceutical Industry – Brochure
Specialized shredding systems make the disposal of Pharmaceutical waste safer and cheaper! In the manufacture of pharmaceuticals, all batches that do not meet the regulatory requirements must be destroyed in accordance with the regulations of chemical and waste ...
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