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History and Milestones

2014

September– Patheon acquired Gallus BioPharmaceuticals

March – DPx Holdings was formed through the merger of Patheon and DPP

2013

January – Dr. Aqeel Fatmi is appointed as Executive Vice President, Global Research & Development and Chief Scientific Officer

2012

December – Acquisition of Banner Pharmacaps, a market leader in soft gelatin capsule technology, adding a new proprietary products and technology business.

December – Geoff Glass appointed as President, Product and Technology Commercialization.

November – Appointment of Michael Lehmann as President, Global PDS.

October – Appointment of Harry Gill as Senior Vice President, Quality and Continuous Improvement.

April – Launch of P-Gels™ line of softgel development and manufacturing services, a partnership with Softigel offering $9 billion capsule available capacity.

March– Patheon Certified Consultants program launches giving customers access to 15 of the industry's top independent consultants.

February – Appointment of Stuart Grant as Executive Vice President, Chief Financial Officer.

January– Appointment of Antonella Mancuso as President, Global Commercial Operations and Chief Manufacturing Officer.

2011

October -- Signed three-year, $18 million development agreement with Boehringer Ingelheim.

September – Established South San Francisco Lab early development center.

August – Appointed Rebecca Holland New as Chief Human Resources Officer and Senior Vice President, HR and Corporate Communications.

July – Appointed Gary L. Shope as Chief of Staff.

May – Appointed Michael E. Lytton as Executive Vice President, Corporate Development and Strategy, and General Counsel.

March– Launched the first backup manufacturing program for sterile products.

February – Appointed James C. Mullen as Chief Executive Officer and to Board of Directors.

January – Launched SoluPath™, the first fixed-price, multi-platform solution to improve bioavailability.

2010

December – Appointed Peter Bigelow as President, North American Operations and Interim Chief Executive Officer.

October – Received 2010 European Outsourcing Award for the most effective scale-up/technology transfer.

June – Expanded manufacturing agreement with Merck & Co., solidifying Patheon as a key preferred supplier, serving the company from eight global facilities.

May – Received 2010 Lilly Sustained Supplier Award for Bourgoin facility's continued delivery of exemplary quality, speed and service.

April – Added Softgel development and manufacturing capability to Cincinnati facility.

April – Appointed Mark Kontny, Ph.D. as President, Global Pharmaceutical Development Services and Chief Scientific Officer.

March – Signed long-term agreement for commercial manufacturing of Contrave® (sustained-release obesity drug), and development of future formulations of Orexigen® products.

January– Announced two, five-year manufacturing agreements with Sanofi-Aventis.

2009

November – Expanded Ferentino, Italy site, adding a sterile pilot plant within a development center, focusing the facility on sterile manufacturing, including aseptically filled, terminally sterilized liquids and lyophilization.

December – First commercial shipments of SUMAVEL® DosePro® (sumatriptan injection) to Zogenix®.

2008

September – Established U.S. headquarters in Research Triangle Park, North Carolina, and European headquarters in Zug, Switzerland.

2007

November – Appointed Wesley P. Wheeler as Chief Executive Officer.

April – JLL Partners, through its investment vehicle JLL Patheon Holdings LLC, complete the purchase of $150 million of convertible preferred shares of Patheon through a private placement.

2006

January – Signed five-year master supply agreement with Merck & Co as a strategic partner for commercial manufacturing and pharmaceutical development services.

2004

December – Acquired MOVA Pharmaceutical Corporation (MOVA), a leading U.S. prescription pharmaceutical contract manufacturer located in Puerto Rico, U.S. MOVA comprised three U.S. FDA-approved facilities, with over 900,000 ft2 (83,600 m2) of solid, liquid, sterile liquid and solid oral cephalosporin manufacturing capacity.

2002

December – Acquired Cincinnati Operations from Aventis (now Sanofi-Aventis). The facility, Patheon's first in the United States, included 372,000 ft2 (34,500 m2) of manufacturing and 85,000 ft2 (7,900 m2) dedicated to development, expanding PDS capacity.

February – Acquired Ferentino Operations outside Rome, Italy, expanding lyophilization capacity and adding Large Volume Parenteral (LVP) manufacturing capabilities. Lyophilization capacity expanded with significant upgrades to Ferentino and Monza Operations.

2001

June– Established PDS facility in Swindon, U.K., enabling integrated development services in both Europe and North America, and adding sterile injectable development capabilities.

May – Acquired Whitby Operations from Novartis Pharmaceuticals Canada. The 193,000 ft2 (17,900 m2) facility increases capacity to manufacture high-volume prescription and OTC products.

March – Opened newly constructed 8,500 ft2 (800 m2) formulation development facility at Toronto Region Operations, expanding PDS capacity and high-potency development capabilities.

2000

September – Acquired remaining 52 percent of the shares of Global Pharm Inc.

1999

December – Acquired two European facilities from Hoechst Marion Roussel Group: Swindon Operations, U.K. and Bourgoin-Jallieu Operations, France. Strengthens European presence with significant increase in prescription manufacturing capacity, and addition of sterile injectable and cephalosporin capabilities.

1998

November– Acquired 300,000 ft2 (27,900 m2) facility in Monza, Italy. The former Boehringer Mannheim facility enables offering of sterile injectable and lyophilized product services.


1997

January- Acquired Toronto Region Operations facility in Mississauga, Canada from Hoffman-La Roche Ltd (former Syntex facility). The 184,000 ft2 (17,100 m2) facility included high-potency capacity for prescription products and modern laboratory facilities to expand pharmaceutical development services (PDS) business. The facility also offered U.S. FDA-approved manufacturing capabilities.

1996

November – Completed fully marketed public offering, raising gross proceeds of C$14.4 million by issuing 11.5 million common shares for C$1.25 per share.

1995

May – Entered prescription and clinical trial materials manufacturing by acquiring 48 percent ownership of Global Pharm Inc. The facility, later renamed Toronto York Mills Operations, had U.S. FDA-approved manufacturing capabilities and was formerly owned by Upjohn of Canada.

1994

Added facility in Burlington, Canada, later renamed Burlington Century Operations.

1993

May– Changed company name to Patheon Inc. (Stock symbol: PTI).

January – Became publicly traded company on the Toronto Stock Exchange.

1990

Began providing pharmaceutical manufacturing services to the U.S. market, capitalizing on the North American Free Trade Agreement (NAFTA).

1982

Expanded operations to Burlington, Canada by forming Promix Laboratories Inc. Facility later renamed Burlington Gateway Operations.

1974

Contract pharmaceutical manufacturing business established as Custom Pharmaceuticals Ltd.

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