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STEMart, a US-based provider of comprehensive services for all phases of medical device development, announced the expansion of its service offerings to include the Bacterial Reverse Mutation Test (Ames) service. This service provides manufacturers and researchers a rapid, cost-effective, and robust method for assessing the mutagenic potential of new chemicals and leachable substances from ...
BySTEMart
As an expert in providing solutions to assist virology and microbiology research, Creative Diagnostics has introduced its efficient and precise Microbial Genome Editing services to support researchers in the modification of specific target genes within an organism's genome.Microbial cell factories are a promising mode of production for fuels, chemicals, and ...
Moreover, industrial biotechnology can benefit from this service by optimizing microbial production of biofuels, pharmaceuticals, and chemicals. As a globally recognized leader in proteomics and metabolomics, Creative Proteomics continues to support researchers in their quest for knowledge. The Central Carbon Metabolism Analysis Service is the latest addition ...
"We sincerely welcome all attendees to visit our booth and explore how we can collaborate to drive innovation and achieve operational success. Our team will be on hand to provide detailed information and discuss tailored solutions to meet your specific needs." Huateng Pharma’s commitment to quality and innovation makes it a ...
Obtaining the Marketing Authorisation Application (MAA) is a key step in the commercialization of drugs in the EU, and also an important help to promote the global market expansion of pharmaceutical companies. The MAA is complicated by the need to consider both European economic integration and the independence of individual member states. As a specialist in regulatory matters, Proregulations has ...
The EU Active Substance Master File (ASMF) is a technical document containing confidential information on an API that is submitted by the manufacturer of the API to the EMA or the medicines regulatory authority of an EU member state. As a form of DMF in the EU, the ASMF is used to support MAA or MAV by manufacturers of pharmaceutical preparations for human or veterinary use. The ASMF applies to ...
U.S. medical device regulations require manufacturers of most class II and a small number of class I devices to file a 510(k) unless they qualify for an exemption. 510(k) is a premarket technical document submitted by the manufacturer to the FDA before the medical device product enters the US market to prove that the product has the same safety and effectiveness in terms of intended use, design, ...
Unlike conventional methods that often rely on labor-intensive and time-consuming practices, Protheragen-ING’s AI-synthesizer is designed to streamline the entire drug synthesis process. At the heart of this innovative solution is its ability to train sophisticated AI models on extensive datasets that include chemical properties, reaction ...
In the world of pharmaceutical ingredients, quality and efficacy has never been more important. ...
With cutting-edge solutions in the field of microneedle technology, Protheragen-ING is on the front lines in this field. As a certified ISO9001 supplier of pharmaceutical ingredients and specialty chemicals, Protheragen-ING keeps innovating to meet the latest market demand. ...
An Abbreviated New Drug Application (ANDA) is an application submitted to the U.S. FDA to demonstrate that a generic drug is equivalent to a previously approved Reference Listed Drug (RLD) in terms of safety, efficacy, and quality. The ANDA contains information used for the review and approval of a generic drug product, and does not typically require preclinical and clinical trial data, but ...
The FDA regulates cosmetics and their ingredients on the U.S. cosmetics market. Strict adherence to FDA regulations and standards is essential for the smooth entry and successful operation of cosmetic products on the US market. At Proregulations, a company that specializes in assisting with regulatory compliance, we offer U.S. Cosmetics Registration services designed to ensure that cosmetics meet ...
Protheragen-ING has recently announced its ability to provide freeze-drying flash-release formulation development services to clients involved in drug discovery and development worldwide. Lyophilized flash-release formulations are advanced drug delivery systems that incorporate the benefits of both lyophilization and flash-release technologies. “Whether customers are trying to develop a ...
In an era where environmental consciousness and sustainability are at the forefront of societal concerns, Alfa Chemistry emerges as a leading provider of biobased pharmaceutical chemicals, plasticizers, and biofuels. These eco-friendly alternatives signify a significant leap toward reducing environmental impact and fostering a sustainable future. Biobased Pharmaceutical Chemicals The realm of ...
Additionally, Huateng Pharma offers tailor-made raw material solutions for the chemical pharmaceutical industry, underscoring its commitment to innovation and quality in pharmaceutical ...
Amerigo Scientific, a distributor focused on providing critical products and services to biomedical and life science communities, unveils the addition of the reliable Daptomycin ReadyMade™ Solution to its growing portfolio of innovative products to power up spectrum and microbiology applications. Daptomycin is an essential antibiotic used in the treatment of serious bacterial infections, ...
Today, Eagle Genomics, the software platform business pioneering the application of network science to biology,?announced its attendance at international tradeshow ACHEMA 2022 in Frankfurt, Germany next week (22-26 August) as a Microsoft Showcase Partner. Eagle Genomics will be featured in Microsoft’s ‘Digital Hub’ Innovation space under the theme “Eagle Genomics and ...
MatTek Life Sciences will produce and distribute EpiOral from its production facility in Slovakia, continuing the BICO groups’ focus on providing on-demand tissues to the European market. MatTek Life Sciences, a Boston-area tissue engineering company and a part of the BICO Group, announced today its European facility in Bratislava, Slovakia, will begin producing and shipping EpiOral, a ...
Because of an increased demand Foeth expanded its range and offers new conical screw “nauta” mixers. Since the launch of this new product line in 2020 clients from Europe to South America have profited from these A-grade new full stainless steel mixers. Features of the new conical mixers Unlike most of its offerings, Foeth’s private label conical screw mixers are brand new. ...
BARNEVELD – Foeth, the Dutch leading European pre-owned process equipment dealer, is helping a major pharmaceutical company in Switzerland to dispose of surplus API production equipment in a sustainable and financially attractive way that became recently available from a production location in Basel. Foeth is responsible to market the re-use of the process equipment to possible end users in ...