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April 08, 2022

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Ensuring Drug Safety through Sterilization of Parenteral Products and Evaluation of Extractables

How do you help ensure that your pharmaceutical product can be released to market as quickly and safely as possible? Some important things you must consider include regulatory expectations, container closure integrity, extractables and leachables, method validation, and sterilization assurance. You can learn directly from our industry experts in Philadelphia on May 11th and 12th. There will be two days full of information and discussion about sterilization and lab testing. Learn more.

	Industry News

Clayton Pharmaceuticals and VistaPharm Receive FDA Approval for Sucralfate Oral Suspension
Clayton Pharmaceuticals has received FDA approval for Sucralfate Oral Suspension with Competitive ... read more »

BMS Receives European Commission Approval for CAR T Cell Therapy Breyanzi for Lymphoma
Bristol Myers Squibb announced that the European Commission (EC) has granted Marketing Authorization... read more »

FDA Updates Sotrovimab Emergency Use Authorization
Sotrovimab is no longer authorized to treat COVID-19 in any U.S. region due to increases in the ... read more »

FDA Approves Novartis Vijoice® for Select Patients with PIK3CA-Related Overgrowth Spectrum
Novartis announced that the U.S. Food and Drug Administration (FDA) granted accelerated approval to ... read more »

	Infographic

Transition to Recombinant rFC for Endotoxin Testing: The Sustainable Choice
Transition to Recombinant rFC for Endotoxin Testing: The Sustainable Choice
Recombinant Horseshoe Crab Factor C (rFC) provides a sustainable, highly effective, and environmentally friendly sustainable means of endotoxin ... read more »

	Featured Articles

Event-Based Sterility Assurance Event-related sterility assurance is, simply put, any event that compromises the integrity of the barrier enclosing the sterilized material. Such ... read more »

Mycoplasma Testing in an Ever-Changing World Mycoplasmas are commensal parasites that can be contaminants of cell cultures and animal-derived products. These contaminants are not as visually ... read more »

	Featured Video

On-Demand Webinar: Mitigating Risk in Manufacturing with Rapid Microbial Monitoring in Pharmaceutical Water
In this webinar we discuss examples of real-world conversations as pharmaceutical customers grapple with true microbial contaminations within their ... watch »

On-Demand Webinar: Sophisticated Formulation Approaches for Insoluble Drug Candidates
The webinar will explain the role nano-formulations play to accelerate the drug discovery/development process. It will also outline a formulation ... watch »

	Featured Products

alpha300 R Confocal Raman Imaging System
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	Featured Whitepaper

eBook: Advanced Research and QA/QC Solutions Using Near-Infrared Spectroscopy
FT-NIR technology offers many advantages over classic wet chemical and chromatographic analysis methods. It is fast, inexpensive and safe because no chemicals are used and various parameters are ... read more »

Whitepaper: Comprehensive Pure Water Guide for Pharmaceutical Engineers
In today’s pharmaceutical facilities the availability of purified water is essential. While the domestic consumer considers tap water to be “pure”, the pharmaceutical end-user regards it as grossly ... read more »

	Events

SMi’s 9th Annual Conference Pre-Filled Syringes East Coast
Boston, MA – 04/25/2022
The global pre-filled syringes market was valued at $1139.6 million in 2020 and with the rapid growth of the industry, is expected to grow at a CAGR ... event details »

SMi’s 22nd Annual Pain Therapeutics Conference
London, UK – 05/04/2022
SMi’s 22nd Pain Therapeutics Conference will cover the leading advances in pain therapeutics, exploring late development clinical trials, novel ... event details »

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