Trac Services | Our Services | TRAC Services
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Our Services

The consultancy for global, pharmaceutical regulatory affairs

TRAC offers a full range of EU Regulatory Affairs consulting services for the global pharmaceutical industry. Our regulatory affairs consultants are specialists in their particular fields and cover all stages of the product lifecycle

Learn more about European Regulatory Affairs

eCTD

TRAC is a company you can trust. We have been creating eCTD submissions since 2008 and have the systems and processes in place for all your eCTD publishing needs.

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Identification of Medicinal Products (IDMP)

Our expertise can help you comply with the EU IDMP legislation.

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Clinical  Trial Applications

With our support and advice you can be confident of meeting your regulatory requirements right from the start.

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Marketing Authorisation Applications

Our knowledge, experience and enterprising approach mean that we will help you formulate a regulatory strategy that works for you, ensuring that your Marketing Authorisation Applications can be compiled and submitted with confidence.

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Post Marketing Maintenance

Our team works hard to provide on-going protection for your investment advising on all of the scientific disciplines required for the maintenance and maximisation of a marketing authorisation.

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Case Studies

We always provide a highly individualised service and are proud of being recognised for going that extra mile to support our clients.

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