Let us help you with international registration.
If the global market is where you want to take your product, SRC can help get you there. Not only do we have the know-how to complete the U.S. regulatory process for antimicrobial and pesticide products, our expertise reaches throughout the world to assist with manufacturing, research, quality control, testing, registration strategy and data substantiation. SRC has experience in Canada (PMRA, TPD, NHPD, CFIA, BCS), Australia (TGA, APVMA), New Zealand, and Thailand. Partnering with regional experts, we are able to negotiate local hurdles in a timely fashion.
Did You Know?
SRC Consultants have the knowledge to help you create a single set of data for global registration.
Don’t risk repeating studies to fit multiple countries’ requirements.
Because our team is well versed in test requirements, we can create a single set of data for global registration. We work with your team to make sure we are using the most cost-effective approach to your study and submission management.
- Household and institutional disinfectants
- Food contact sanitizers
- Treated articles
- Disinfectant and antiseptic towelettes
- Health care personnel hand washes
- Hand sanitizers
- Pool/spa products
- Fungicidal claims
- Nonfood contact sanitizers
- Ingredient status
- Submission development
- Initial registration
- Data development strategy
- Registration/regulatory strategy
- Study design and protocol development
- Data interpretation
- Label development, review, and preparation
- GLP compliance
- Registration and compliance
- Data requirements
- Problem solving
- Regulation interpretation
- New inert submissions
- New protocol submission
- Website/sales literature review
- Global substantiation strategy
Scientific and regulatory strategies for biocidal and pesticidal products.
Extensive experience in FDA antimicrobial drug and device offerings.
Comprehensive state registrations and tracking services.
Data development and management for efficacy, chemistry, and toxicology.
Global registration strategies and substantiation.
Ingredient list cross-referencing and disclosures.
Safety Data Sheets
Analysis for proper hazard classification and communication.
Experience in R&D, quality, auditing, and organic materials registration.