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ATMI: Single-Use Could Replace Multi-Use, as Potency Increases

ATMI: Single-Use Could Replace Multi-Use, as Potency Increases

Eric Isberg

Global Product Manager - ATMI

Single-use is set to dominate biopharma processing as products become more potent resulting in smaller volumes, according to ATMI.

Published: 15-May-2013

Tech and Regulatory Issues? Biotech/Manufacturing Firms Discuss

Tech and Regulatory Issues? Biotech/Manufacturing Firms Discuss

Purification bottlenecks, integrating single-use technologies and low cost companies are just some of the issues affecting the biotech industry today, according to experts at this year’s Interphex.

Published: 29-Apr-2013

IHolland Talks Tabletting Solutions for Sticky Formulations

IHolland Talks Tabletting Solutions for Sticky Formulations

Clare Taylor

IHolland says tableting-focused research project will save customers time and money.

Published: 24-Apr-2013

Almac Talks Facility Expansions on Both Sides of the Atlantic

Almac Talks Facility Expansions on Both Sides of the Atlantic

Jim McGibbon

Almac says $10m investment at its recently expanded facility in Northern Ireland compliments the sites existing formulation development capabilities.

Published: 24-Apr-2013

Happy holidays from William Reed Business Media!

Happy holidays from William Reed Business Media!

The working year is almost done, time to pause from ‘the business’ and embrace the festive season…go on, give it a big hug. Happy holidays!

Published: 19-Dec-2012

Price of water & corporate sustainability agendas pushing waste reuse; Veolia

Price of water & corporate sustainability agendas pushing waste reuse; Veolia

Johann Bonnet

Strategic Account Manager - Veolia

The price of water and corporate agendas are driving pharmaceutical production plants to reuse and reclaim waste, Veolia said.

Published: 21-Jun-2012

Freeman updates powder analysis tech

Freeman updates powder analysis tech

Tim Freeman

CEO - Freeman Technology

Freeman Technology has added a new “intuitive” control system to its multi-purpose powder analysis system.

Published: 20-Jun-2012

ATMI gears up for single-use "boom" for biotech industry

ATMI gears up for single-use "boom" for biotech industry

Brent Todd

Regional sales manager - ATMI

ATMI has added helium integrity testing of bioprocess vessels in response to what it says is a boom in the single-use technology arena.

Published: 18-Jun-2012

Mettler Toledo take track and trace offering to the US

Mettler Toledo take track and trace offering to the US

Janice Wortham

Regional sales manager, pharmaceutical - Mettler Toledo

Mettler Toledo is taking its ramped-up track and trace offering to the US in a bid to plug what it says is a sizeable gap in the market.

Published: 14-Jun-2012

Open pharma – regulator talks “critically important” to ending shortages; FDA

Open pharma – regulator talks “critically important” to ending shortages; FDA

Jeffrey Baker

Deputy Director, Office of Biotechnology Products, CDER - FDA

Biopharma firms can overcome a hurdle to ending drug shortages by having transparent talks with the FDA, an Agency official said.

Published: 11-Jun-2012

Fantastic four pool together to create super suite for processing HP drugs

Various

Various - Schenck Accurate, PSL, Malvern, Sturtevant

Schenck Accurate, Malvern, PSL and Sturtevant have teamed up to create a “unique” new turnkey isolated milling suite which they say will wipe out unnecessary waiting times for high potency (HP) drug processing.

Published: 05-Jun-2012

P-Gels mean cheaper and more varied drug development, says Patheon

P-Gels mean cheaper and more varied drug development, says Patheon

Geoff Glass

VP of sales and marketing - Patheon

Patheon says its new soft gel platform is creating cheaper development opportunities for drugsmakers.

Published: 31-May-2012

Mergers a “key problem” for regulatory compliance, drug quality expert says

Mergers a “key problem” for regulatory compliance, drug quality expert says

Rosario Quintero-Vives

Senior Regulatory & Compliance Specialist - RQV Consultants

Biopharma mergers are a “key problem” for manufacturing quality teams as the loss of focus can lead to regulatory actions, a compliance expert said.

Published: 29-May-2012

EMD Millipore stresses ease of use and flexibility benefits of new bioreactor

EMD Millipore stresses ease of use and flexibility benefits of new bioreactor

Mani Krishnan

director Mobius single-use processing systems - EMD Millipore

EMD Millipore premiered a new single-use bioreactor at Interphex 2012, claiming the new design addresses industry demand for ease of use and flexibility.

Published: 21-May-2012

PTI stresses benefits of non-destructive testing at Interphex

PTI stresses benefits of non-destructive testing at Interphex

Oliver Stauffer

VP Inspection Technologies - PTI, LLC

PTI says its new non-destructive testing technology is uniquely positioned to help manufacturers reduce waste and save time and money.

Published: 15-May-2012

in-Pharmatechnologist.com's review of Interphex 2012

in-Pharmatechnologist.com's review of Interphex 2012

in-Pharmatechnologist.com was at Interphex 2012 in New York, US to launch the revamped version of our website and speak to the pharmaceutical manufacturing and processing tech sector’s movers and shakers.

Published: 10-May-2012

in-Pharmatechnologist @ Interphex 2012

in-Pharmatechnologist @ Interphex 2012

In-Pharmatechnologist.com has chosen Interphex - the drug industry’s biggest production and processing technology show – as the launch event for our new look, refocused news website.

Published: 24-Apr-2012

Parexel discusses transdermal drug delivery techs

Parexel discusses transdermal drug delivery techs

Ravi Harapanhalli

Principal Consultant and Practice Lead for Late Stage Product Development Parexel Consulting - Parexel

Electroporation is the wave of the future for transdermal drug delivery, according to Parexel’s Ravi Harapanhalli.

Published: 22-Dec-2011

“Fear of the unknown” limiting adoption of real-time release testing, FDA says

“Fear of the unknown” limiting adoption of real-time release testing, FDA says

Christine Moore

Acting Director, Office of New Drug Quality Assessment - FDA

Real-time release testing can save money by cutting recalls but “fear of the unknown” is limiting use, a FDA official said.

Published: 21-Nov-2011

Pharma must improve existing methods to boost solubility as “quantum leap” unlikely

Pharma must improve existing methods to boost solubility as “quantum leap” unlikely

Graham Buckton

CEO - Pharmaterials

To boost solubility pharma must develop, refine and improve existing methods as a “quantum leap” in formulation is unlikely, Pharmaterials' CEO said.

Published: 15-Nov-2011

FDA developing QbD examples to ready generic industry for 2013 deadline

FDA developing QbD examples to ready generic industry for 2013 deadline

Lawrence Yu

Deputy Director, Science and Chemistry - FDA

The US FDA is publishing immediate and modified release QbD examples to help generics companies prepare for full implementation in 2013.

Published: 10-Nov-2011

Pfizer & Bend collaborating on osteoarthritis nanoparticle drug delivery

Pfizer & Bend collaborating on osteoarthritis nanoparticle drug delivery

Michael Morgan

Director of New Technologies - Bend Research

Bend Research is developing a nanoparticle drug delivery system for treating osteoarthritis in a “close collaboration” with Pfizer.

Published: 03-Nov-2011

ImQuest Biosciences launches ARV delivery patch at AAPS

ImQuest Biosciences launches ARV delivery patch at AAPS

Anthony Ham

Lead researcher - ImQuest

A new antiretroviral (ARV) transdermal delivery patch developed at ImQuest Biosciences will wipe out the need for the “cocktail” of oral medication HIV sufferers have to take every day.

Published: 27-Oct-2011

Round-up of SAFC's Glasgow conference

SAFC

SAFC will extend its focus on high potency production through a number of new investments.

Published: 03-Oct-2011

DSA talks social media in pharma at DIA 2011

DSA talks social media in pharma at DIA 2011

Elizabeth Garrard

Chief Safety Officer - DSA

Social media can play a role in ensuring that medicines are safe, but regulatory input is needed according to the Drug Safety Alliance (DSA).

Published: 23-Jun-2011