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Product Testing & Registration
Reduce Your Regulatory Burden
As government regulations around the globe tighten on new and existing products, timelines become increasingly more difficult to meet and complying with these mandatory regulations becomes increasingly complex.
Regulatory approvals take time, energy and money. They are often extremely complicated and require advanced scientific training. When not pursued strategically or processed with absolute accuracy, they can set you back months or even years. As government regulations around the globe tighten on new and existing products, compliance becomes increasingly complex.
Focused Solutions
GLOBALTOX has a team of expert scientists and regulatory affairs professionals who understand the regulations, can help determine your testing and information requirements, and can manage the whole regulatory process on your behalf in a timely and efficient manner.
GLOBALTOX specializes in preparing regulatory submissions and providing compliance support for companies with interests in:
- Chemicals and Polymers
- Organisms
- Natural Health Products/Dietary Supplements
- Pharmaceuticals
- Cosmetics
- Pesticides
- Foods
We are highly qualified and have built trusted relationships with regulatory officials in multiple jurisdictions. Our approach is comprehensive and scientifically sound. With GLOBALTOX, you can be confident that you are making solid business decisions to address your regulatory burden.
GLOBALTOX has also developed a web-based focused solution for chemical and polymer management in Canada: CAPCCAT.
CAPCCAT is a Chemical and Polymer Comprehensive Compliance Assessment Tool that was developed by GLOBALTOX in response to the complexity of compliance with CEPA '99. Canadian regulation of chemicals and polymers has evolved from simple industrial substance management using the Domestic Substances List (DSL) and Non-Domestic Substances List (NDSL), to a much more complex regulatory system integrating the management of a wider range of substances and numerous risk management measures, both currently imposed and under development.
Your Advantages with GLOBALTOX
» Experience, to optimize your approach
Our multi-disciplinary team is your major asset. Having represented hundreds of clients in consultations with regulatory officials, we optimize your strategies while helping you avoid costly errors.
» Relationships, to leverage on your behalf
Strong relationships propel success. After many years in product testing and global registration, GLOBALTOX has earned the respect of regulatory officials. Our credibility has been further strengthened by our vocal and valued membership in industry associations. As our client, you benefit from these crucial relationships.
» Defensible Science, to ensure a quality submission
Getting it right the first time is vital. GLOBALTOX scientists ensure that all data presented to regulators will withstand rigorous scrutiny; greatly improving your chances for seamless product approval.

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Optimize Your Return on Investment
Value in regulatory consulting is directly related to process efficiency. With GLOBALTOX, you get a highly efficient, carefully planned, client-centric solution designed by experts to expedite regulatory approval. We deliver an approach that balances the cost of acquiring data with your need for regulatory compliance.
Let GLOBALTOX be your guide through the complexities of government regulations. With our understanding, strategically applied, your regulatory burden will quickly become a focused regulatory solution. Your investment in good advice will pay off in market advantage.
Proven Results!
For more specific information on our various areas of expertise, please click on the appropriate heading in the menu to the left.
Global Regulatory Compliance Services
- Regulatory needs assessment and strategic planning to support product development and registration.
- Generation of technical data to meet registration requirements.
- Development of the justification for the use of alternative procedures, surrogate data, and testing waivers.
- Preparation of comprehensive regulatory dossiers.
- Management and co-ordination of all aspects of product submission processes.
- Delivery of customized training programs that translate complex regulatory frameworks into language which is easily understood and applied.
- Co-ordination of communications with government agencies, including pre- and post-regulatory consultations.
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