Fine-Chemical Producers Make Targeted Investments - Pharmaceutical Technology

Latest Issue

Latest Issue
PharmTech Europe

Fine-Chemical Producers Make Targeted Investments
Contract API manufacturers proceed with select investment in capacity and service additions.

Pharmaceutical Technology
Volume 37, Issue 4, pp. 114-116

Other developments

Several companies have announced overall manufacturing capacity additions. For example, Albemarle is expanding its manufacturing facility in Tyrone, Pennsylvania. The $30-million expansion builds on an earlier expansion that began operations in November 2012, which will result in an eventual 40% increase in reactor capacity for the company’s custom-manufacturing business. The first increment of new capacity will be operational late in the first quarter of 2014.

In February 2013, PharmaZell added an additional manufacturing site to its European manufacturing network. The company acquired a manufacturing site in Liestal, Switzerland previously operated by AbbVie (formerly Abbott). Abbott’s pharmaceutical business was spun off in a separate company, AbbVie, in January 2013. The Liestal site consists of multipurpose manufacturing equipment with 150 m3 of reactor volume with drying and milling capacity, packaging cleanrooms, a pilot plant, quality-control laboratories, and warehouses for manufacturing small-molecule, large-volume APIs.

In 2012, Almac expanded its API manufacturing facility at its European headquarters in Craigavon, United Kingdom, with a scheduled completion for the end of 2012. The upgrade included installation of two 1000-L reactors and a pressure-filter dryer, which allows production of GMP APIs up to 150-kg batches.

In September 2012, Cambridge Major Laboratories (CML) reported that it is expanding its large-scale API manufacturing facility in Germantown, Wisconsin. The expansion comes three years after commissioning the new site. The expansion includes additional reactor capacity and isolation equipment as well as additional investments in engineering controls. Also, in 2012, Cedarburg Hauser Pharmaceuticals expanded its capacity at its Wisconsin-based API manufacturing plant and made additional upgrades for improving safety and GMP systems.

Other companies are making targeted investment in select manufacturing activities. In 2012, Dr. Reddy’s Custom Pharmaceutical Services expanded its activated mPEG manufacturing capabilities at is facility in Mirfield, United Kingdom. SAFC, part of Sigma-Aldrich, is expanding its operations in Scotland by investing in the development of a new powder-manufacturing facility at its Irvine site. SAFC’s new facility in Irvine is its second powder manufacturing facility, which will support SAFC’s risk- management program, which provides an internal back-up supplier for its customers. The new facility will be used to serve customers across Europe.

Almac and DSM Pharmaceutical Products recently reported the successful transfer of enzymes for enzyme screening, process development and scale-up as part of the companies’ agreement in biocatalysis, which was announced in October 2012. The agreement grants both companies access to their enzyme platform technologies and services for the manufacturing of APIs. The collaboration also enables Almac to offer its customers a preferred partner for large-scale production. In February 2013, DSM Pharmaceutical Products signed an agreement with Chemtrix, a supplier of flow-chemistry equipment and services, for providing equipment, development and manufacturing services to the pharmaceutical industry. Chemtrix specializes in ready-to-use laboratory and kilo-scale microreactors as well as reactor and process design for industrial reactors. DSM provides drug-synthesis route development, scale-up, and implementation of continuous-flow processes for manufacturing. DSM has FDA approval for using microreactors for making a pharmaceutical product at commercial scale under cGMP at its facility in Linz, Austria, where its dedicated commercial-scale installation is located. The DSM–Chemtrix collaboration will initially offer an industrial flow process- development package for customized scalable flow-chemistry solutions. The package covers all phases of process design, scanning chemistries, chemistry development, route scouting, equipment design, and scale-up for fully continuous or integrated processes.

Ajinomoto plans to invest approximately JPY 1.3 billion ($13.9 million) to double production capacity for amino acids for use in pharmaceuticals and foods at its subsidiary Shanghai Ajinomoto Amino Acid in Shanghai. The expansion is scheduled to come on line in October 2013. Ajinomoto estimates the current global market for amino acids for pharmaceuticals and foods at 30,000 tons, and with growth in emerging markets, expects demand to rise to 45,000 tons by 2020. Several fine-chemical producers and contract API producers also recently announced activity in support of finished product manufacturing. For example, earlier this year, Ajinomoto agreed to acquire Althea Technologies, a San Diego-based contract provider of fill–finish services. Aesica and the CDMO EmulTech are partnering on the commercial development of ET4ME, an emulsion technology for product formulation. ET4ME is a microencapsulation technology that uses a microfluidic process to create a measurable microparticulate suspension. The technology can be used for small molecules and biologics.

Cambrex agreed to contract manufacture Dow Chemical’s hydroxypropyl methylcellulose acetate succinate, an excipient provided by Dow as part of a solubilization partnership that Dow and Bend Research formed in 2012 under which Dow is commercially supplying solubility-enabling excipients. Cambrex has begun construction of the new facility at Cambrex’s site in Karlskoga Sweden with commercial product availability set for year end 2013. In another development, ScinoPharm and Foresee Pharmaceuticals agreed to form a joint venture to develop a series of peptide injectable drugs, with the first being a leuprolide injectable drug product, by which leuprolide will be formulated in a proprietary controlled-release drug delivery system originally developed by Foresee and transferred to the joint venture. ScinoPharm is investing $3.6 million for a minority ownership in the new company.


blog comments powered by Disqus
LCGC E-mail Newsletters

Subscribe: Click to learn more about the newsletter
| Weekly
| Monthly
| Weekly

What role should the US government play in the current Ebola outbreak?
Finance development of drugs to treat/prevent disease.
Oversee medical treatment of patients in the US.
Provide treatment for patients globally.
All of the above.
No government involvement in patient treatment or drug development.
Finance development of drugs to treat/prevent disease.
Oversee medical treatment of patients in the US.
Provide treatment for patients globally.
All of the above.
No government involvement in patient treatment or drug development.
Jim Miller Outsourcing Outlook Jim MillerOutside Looking In
Cynthia Challener, PhD Ingredients Insider Cynthia ChallenerAdvances in Large-Scale Heterocyclic Synthesis
Jill Wechsler Regulatory Watch Jill Wechsler New Era for Generic Drugs
Sean Milmo European Regulatory WatchSean MilmoTackling Drug Shortages
New Congress to Tackle Health Reform, Biomedical Innovation, Tax Policy
Combination Products Challenge Biopharma Manufacturers
Seven Steps to Solving Tabletting and Tooling ProblemsStep 1: Clean
Legislators Urge Added Incentives for Ebola Drug Development
FDA Reorganization to Promote Drug Quality
Source: Pharmaceutical Technology,
Click here