Displaying 26–50 of 309 results for USP
Well-known shortcomings of customary, online weight measurements systems are discussed, especially for industrial applications in the pharmaceutical industry.
New techniques are expanding the role of X-ray analytical technologies to range from drug discovery to quality control
In-process testing for contaminants is only as good as the methods used, so employing carefully developed and validated protocols is essential
Parenteral drug manufacturers are sharpening capabilities and coming into their own
International Conference on Harmonization represents the countries interested in unified standards
The company announced the U.S. launch of Doxycycline Hyclate Delayed-Release (DR) Tablets USP, 50 mg
Misdirection in the implementation of isolation technology
Due to the presence of a particulate, Hospira is voluntarily recalling one lot of 8.4% Sodium Bicarbonate Injection, USP
The complexity of biologics makes it imperative to consider some tough questions that need asking when seeking a more specialized large molecule CMO.
Neither rain, nor sleet, nor snow could keep me from finding the lastest technology at IFPAC 2016 conference.
Ensuring compliance for raw material identification is easily within reach
Why LER is here to stay, the need to safeguard test supply, revisiting the definition of alternative assays, and moving toward automation
The product contains an inactive ingredient that may cause nasal burning if OXAYDO is manipulated
This product is a combination penicillin-class antibacterial and beta-lactamase inhibitor
Humans invading your sterile processes? Advances in aseptic processing technologies aim to keep their risk and contamination at bay.
Should an API manufactured by biological or biotechnological process be consider not sterile?
Drug Owners and CMOs both have skin in the game when it comes to specifying bioreactor technology
Fewer headaches, reduced complexity and flexibility come with the territory
USP  assigns "specific responsibility" to the manufacturer. In the case of contract
eBook on meeting USP and EU GDP regulatory requirements. Learn the latest revisions from the U.S. Pharmacopeial Convention (USP) Good Distribution Practices (GDP) according to the European Commission.
The advantages of near-infrared spectroscopy in pharmaceutical analysis
BioPure, a Watson-Marlow Pumps Group company, specializes in single-use bioprocessing components for end users and OEMs, including its range of BioBarb® hose tail to Tri-Clamp adaptors.
Reducing process related failures and quality costs; Continued Process Verification can improve control and lower failure rates
This executive summary from GE Analytical Instruments discusses an advancement in Conductivity analysis technology that can significantly reduce the time spent to comply with the USP <645> regulation.