Jun 10 2018

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Pharmaceutical formulation companies

Methods for Identifying Out-of-Trend Data in Analysis of Stability Mea.

Pharmaceutical formulation companies

Selecting the Appropriate Technology for Oral Bioavailability Enhancem.

Pharmaceutical formulation companies

Comparing Endotoxin Detection Methods

Pharmaceutical formulation companies

Establishing an Effective Data Governance System

Pharmaceutical formulation companies

Patient Centricity Takes Center Stage

Pharmaceutical formulation companies

Moving Toward Direct-to-Patient Models

Pharmaceutical formulation companies

Operational Best Practices

Pharmaceutical formulation companies

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Top News

EMA to Relocate to New HQ in Amsterdam in Wake of Brexit

Nov 21, 2017

Following a vote by member states in favor of Amsterdam as the agency’s new headquarters, the relocation will take place over the next 16 months, with operations expected to start up in March 2019.

FDA Approves Digital Pill

Nov 14, 2017

The agency approved Abilify MyCite, a pill with a sensor that digitally tracks if patients have ingested their medication.

FDA to Recognize Inspections from EU Drug Authorities

Oct 31, 2017

A mutual recognition agreement to accept inspection data from eight EU regulatory authorities may reduce inspection burdens at global drug facilities.

PharmTech eBook Series

Biologics and Sterile Manufacturing 2017 eBook

Pharmaceutical formulation companiesNew technologies, including single-use systems, are leading the push for faster production and higher titers. At the same time, ensuring quality in raw materials and water systems, and controlling contamination are paramount. In this Biologics and Sterile Manufacturing eBook, the editors explore key technology, process, and operational topics.

Industry News

EMA to Relocate to New HQ in Amsterdam in Wake of Brexit

Nov 21, 2017

Following a vote by member states in favor of Amsterdam as the agency’s new headquarters, the relocation will take place over the next 16 months, with operations expected to start up in March 2019.

Novartis, ASCP, and ACS Partner for African Cancer Initiative

Nov 16, 2017

The entities announced that they will partner to improve access to cancer treatments and diagnostics in Ethiopia, Uganda, and Tanzania.

CPhI Global Pharma Index Shows India’s Reputation Improving

Nov 16, 2017

India was ranked by international pharmaceutical companies as the third most competitive nation globally.

Supplier News

Design Solution for Single-Use Technology Applications

SciLog Select Go Single-Use Assemblies from Parker Hannifin uses an assortment of validated parts and assemblies to build needed devices for biopharmaceutical manufacturing.

Avista Doubles API Manufacturing Capacity at Colorado Facility

Avista Pharma Solutions facility and equipment upgrades at its Longmont, Colorado facility support processing of potent compounds.

Integrated Analytical Software Solutions for Clinical and Regulatory Processes

MasterControl has added three new cloud-based analytical solutions to its MasterControl Version 11.7 software for clinical managers and regulatory/submissions professionals.

Bio/Pharma News

FDA Approves Roche’s Hemophilia A Biologic and Expands Indication for Leukemia Drug

The agency has approved a biologic-based new molecular entity for treating hemophilia A and has expanded the indication for a leukemia drug to now treat a common form of non-Hodgkin lymphoma.

Samsung Bioepis Receives Approval for First Trastuzumab Biosimilar, Ontruzant, in Europe

Ontruzant is the first biosimilar of Roche’s Herceptin (trastuzumab) to be approved in Europe.

Boehringer Ingelheim Launches Open-Access Platform of Selected Preclinical Molecules

The platform offers scientists access to best-in-class molecules supported by comprehensive data packages.


FDA’s Policy on Regenerative Medicine Therapies

Commissioner Scott Gottlieb, MD, outlined a plan to support innovation of regenerative medicines while ensuring public safety.

Gottlieb Sends Message About REMS and Market Competition

FDA is exploring ways to keep branded drug companies from using REMS to block the development of generic drugs.

FDA Works to Get Pharma Up and Running in Puerto Rico

While most pharma companies are in partial production using generators, few are operating at 100% capacity.

Drug Development

ADC Targets Fail Because of Aggregation Problems

ADC Bio experts warn of impending problems in the ADC pipeline with millions wasted in development costs.

Pharmaceutical formulation companies

Growing Demand for Taste-Masking Technologies

Taste masking increases drug acceptability and medication adherence in pediatric, geriatric, and other special patient populations.

Awards Recognize Industry Contributions

Industry experts were honored for business, scientific, and social contributions.

Best Practices

Best Weighing Practices in the Pharmaceutical Industry

Understanding what affects a measurement and implementing appropriate procedures will aid weighing accuracy.

Maintaining Thermal Fluid Systems

Preventative maintenance of heat transfer fluid systems is important for reducing downtime in pharmaceutical manufacturing.

Treating Halogenated Hydrocarbon Emissions from Pharmaceutical Production

Regenerative thermal oxidation (RTO) has become a common solution to treat volatile organic compounds (VOC) and hazardous air pollutants (HAP) present in the emissions of many pharma production processes. Regenerative thermal oxidation devices used to treat halocarbons should be designed to prevent corrosion. Anguil Environmental Systems explains best practices for addressing potential fail points in the materials of construction when designing process emission handling systems.

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