Regulatory Affairs

Featured Publication: PLC Life Sciences
Contacts

Tilleke & Gibbins paves the way for life sciences clients to enter and excel in markets throughout Southeast Asia. From research and development and clinical trials to registration and market entry to commercialization and technology transfer, we assist leading and soon-to-be-leading companies through every stage of a product’s life cycle. And when shifting government policies threaten progress, we step in, build coalitions, and facilitate positive change.

Our dynamic group is built on decades of practice in the region and is committed to keeping pace with discovery and innovation. Our client teams are led by experienced attorneys and specialized practitioners and include, as appropriate to the client and its industry, pharmacists, agricultural consultants, and other regulatory specialists. We guide our clients through the layers of formal and informal rules, policies, and procedures, and help our clients forge constructive relationships with regulatory authorities.

Tilleke & Gibbins’ Regulatory Affairs group consistently earns the trust of top companies in the pharmaceutical, cosmetics, consumer products, food and beverages, biotech, medical devices, veterinary products, and other life sciences sectors. Our practice spans the following disciplines:  

  • Clinical Trials and Consumer Testing 
  • Food and Drug Administration (FDA) Registration
  • FDA Import, Export, and Manufacturing Licenses
  • Ministry of Agriculture (MOA) Crop Care Registration
  • MOA Animal, Aquatic, and Hazardous Substance Registration
  • MOA Import, Export, and Manufacturing Licenses
  • Holding Licenses 
  • Regulatory Compliance and Maintenance 
  • Labeling and Advertising Clearance
  • Intellectual Property
Among our recent matters, we have: 
 
  • Acted as counsel to a major pharmaceutical company, which representation included liaising with the Thai FDA on marketing compliance issues, verifying that the client’s marketing activities were in compliance with the complex regulations governing pharmaceutical practice in Thailand, and preventing and mitigating risk and loss.

  • Helped a multinational food company comply with Thai FDA requirements. Advised the client on advertising and promotional materials in Thailand, with particular emphasis on the requirements of the FDA and the consequences of improper ad content.

  • Acted on behalf of a major U.S.-based agrichemical manufacturer. The case involved termination of the client’s distributor for breach of contract and IP (patent and trademark) infringement. In addition, we represented the client in re-registration of its full range of products with the Thai Ministry of Agriculture.

  • Negotiated with the Thai FDA to reclassify a client’s drug product from a new chemical entity (NCE) to new combination (NCO) and secured the successful registration of this product.

  • Answered a critical client inquiry on whether their products could be imported without a certificate of formula disclosure provided to the Customs officer.

  • Secured an export license for the client in an efficient manner, as required by the head of the product group.

  • Coordinated the actions of multiple parties (the reviewers in Thailand, the foreign regulatory affairs authority, and the firm) to timely secure a pharmaceutical product license for the client.

  • Helped an Italian pharmaceutical company prepare an application dossier and obtain a license to operate in the area of medicinal products.

  • Handled a portfolio of products of a pharmaceutical client.  Our representation included assisting in the registration of the products, reviewing and advising on product labels, and assisting in transferring the products to a third company.

  • Secured medical device registration for a top shoe manufacturer and trader in Thailand by giving beneficial advice to the client and working closely with the client to resolve issues with its application. 

  • Registered, in a seamless and efficient manner, a cosmetic product for a large importer in a limited period of time, which enabled the client to timely launch the product.

  • Advised a global pharmaceutical company on all aspects of doing business in Vietnam, including the formation and operation of a representative office, registration as a foreign pharmaceutical company, property transactions, and employment termination and labor disciplinary procedures.

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Namesort icon Position Office Contact

Alan Adcock

Partner Bangkok

alan.a@tilleke.com

+66 2653 5871

Areeya Pornwiriyangkura

Associate Bangkok

areeya.p@tilleke.com

+66 2653 5882

Atthachai Homhuan

Regulatory Consultant Bangkok

atthachai.h@tilleke.com

+66 2653 5610

Darani Vachanavuttivong

Partner Bangkok

darani.v@tilleke.com

+66 2653 5888

Dung Thi Kim Vu

Patent Specialist Hanoi

kimdung.v@tilleke.com

+84 4 3772 5554

Jim Dao

Consultant Ho Chi Minh City

jim.d@tilleke.com

+84 8 3936 2062

Kien Trung Trinh

Associate Hanoi

kien.tt@tilleke.com

+84 4 3772 5567

Michael K. Lee

Partner Ho Chi Minh City

michael.l@tilleke.com

+84 8 3936 2069

Paul G. Russell

Of Counsel Bangkok

paul.r@tilleke.com

+66 2653 5540

Pornsroung Saerekul

Regulatory Consultant Bangkok

pornsroung.s@tilleke.com

+66 2653 5606

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Date Title
April 22, 2011

Clemence Gautier to Speak on Clinical Trials

On May 20, 2011, Clemence Gautier, Consultant, Intellectual Property, will speak at what has been billed as the most comprehensive forum on clinical trials in Thailand. Clinical Trial Forum...

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February 1, 2011

PLC Which Lawyer Names the Firm’s IP Group a Leading Practice in Thailand

Darani Vachanavuttivong, Alan Adcock

In February of 2011, PLC Which Lawyer named the firm’s IP group a leading practice in Thailand, with the firm’s regulatory affairs practice, serving clients in the life sciences, also...

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February 14, 2011

PLC Which Lawyer Endorses Tilleke & Gibbins Attorneys

Alan Adcock, Darani Vachanavuttivong, Srila Thongklang, Sriwan Puapondh, Thawat Damsa-ard

The Practical Law Company’s PLC Which Lawyer publication, regarded worldwide as the essential guide to lawyers and law firms in more than 110 countries, has endorsed the following Tilleke...

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January 24, 2007

Thailand: Critical Need for New Investment

This extensive feature covers a wide range of issues for Thailand’s pharmaceutical industry. Comments from Edward Madden and Edward Kelly of Tilleke & Gibbins are included in the feature.

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February 2, 2007

Interview with Edward Kelly, Edward Madden, and Tiziana Sucharitkul

Tiziana Sucharitkul

This interview of Edward Kelly, Edward Madden, and Tiziana Sucharitkul covers a broad range of topics dealing with the overall intellectual property situation in Thailand, the impact of expected...

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Date Title
July 6, 2009

Claims for Food Products

Paul G. Russell

Recent years have witnessed a proliferation in the number of products available under the “nutritional food” heading. For companies to stand out from their competitors in this growing sector,...

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July 6, 2009

Combating Generics: Rising Pharmaceutical Patent Litigation Trend

Siraprapha Rungpry

In recent years, Thailand has seen an increasing number of pharmaceutical patent litigations, launched by drug originators to combat infringing generic products in the market. This article looks...

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January 15, 2010

Expediting Product Registration at the Thai FDA

Paul G. Russell

Before being marketed in Thailand, a wide variety of products must be registered at the Thai Food and Drug Administration (FDA). These products range from food, food supplements, beverages...

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January 14, 2010

PLC Life Sciences Cross-border Handbook 2009/10 – Thailand Chapter

Areeya Pornwiriyangkura, Paul G. Russell, Siraprapha Rungpry

Written in a Q&A format, this chapter provides a comprehensive overview of the issues faced by life sciences companies in Thailand. Topics covered include the regulatory framework,...

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December 24, 2009

Precautions for License Holders under the Medicine Act

Weerawat Distapinyo

In Thailand, the importation, manufacture, and sale of medicine is governed by the Medicine Act B.E. 2510 (1967). The Act also stipulates the requirements/procedures to apply for a license to...

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