Biocides Compliance Consultation

The “Chemical Product Safety Act” is composed of two parts, management of consumer chemical products, and management of biocides(substances + products + treated products). Consumer chemical products must have their compliance with safety standards according to type be confirmed by designated testing/inspection facilities, and must have their safety certification number printed on the product.
Biocides and biocidal products must receive approval from the government before being released to the market.

Major services provided in regards with biocides

 Joint approval for existing biocides subject to grace period for approval

- Submit application plan for substance approval
- Join CICO, sign agreements
- Analysis and selection/purchase/generation of joint submission data
- Preparation and submission of approval application data
- Follow-up monitoring

 Application for approval of biocides/biocidal products

- Professional advice regarding confirmation of law application, approval of substances/products, need for application for recognition of comparability/similarity
- Confirmation of biocide constituents and identifiable information
- Data gap analysis
- Analysis of test exemption data, preparation of technical documents proving exemption
- Preparation and submission of approval application data
- Maintenance/monitoring after completing approval

 Exclusion from law application of approval, etc.

- Confirmation of exclusion of law application
- Preparation and submission of application data for exclusion of law application

 Performing representative roles and services

- Application for substance approval
- Application for alteration of substance approval, and alteration notifications
- Application for recognition of substance comparability
- Notification for grace period for approval of existing biocidal substances
- Submission of application plan for substance approval
- Application for product approval
- Application for alteration of product approval, and alteration notifications
- Application for special exceptions in product approval
- Application for recognition of product similarity
- Reporting and taking measures regarding new risks, etc.
- Service regarding submission of application plan for substance approval
- Service regarding individual submission of substance approval application data
- Service regarding requests for confidentiality claim
- Service regarding consent for data use

 Test monitoring

- Data gap analysis
- Designing test methods
- Recommendation of Korean and overseas GLP or accredited labs
- Test arrangement and monitoring

 QSAR and Read Across

- Providing strategies for submission of non-test (predicted) data
- Read Across approach via data on substances with analogous structures

 Preparation and update of risk assessment data regarding health/animals/environment

 Translation services in English and Japanese


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