উপাদান সম্মতি পরিচালন সফ্টওয়্যার

ComplyDoC is an intelligent IT and first ever open source code cloud solution for Supply Chain sustainability & product compliance Management to collect information from suppliers.

The strategy mentioned in standard IEC 63000 is considered the most common practice to comply with restricted substances legislations for products.

Suppliers will be asked to sign declarations according to the requirements of standard IEC 62474. The quality of collected declarations should be checked according to requirements of ISO 17050.

Engaging suppliers can save the manufacturer testing cost and limit the amount of testing for mitigation high risk withing the supply chain.

With our international team and deep experience in managing restricted substances within the supply chain, we are able to manage complex supply chain and reduce the intrinsic risk within your supply chain and protect your brand name and sales from non-compliance issues.

ComplyDoC and ComplyMarket supply chain team can take over your process and do the data collection according to IEC 62474, validation collected data according to ISO 17050, and management & reporting the data using our ComplyDoC Software.

At ComplyMarket, we use in addition the Material Declaration Management standard IPC-1752B for managing collected information from suppliers and for preparing Dossiers for the SCIP database.

ComplyMarket  has a dedicated international team for supply chain chemical managements.

ComplyDoC Software and database can cover the following modules:

1. RoHS Directive 2011/65/EU and delegated Directive (EU) 2015/863
2. Substances of Very High Concern (SVHC) of the REACH Regulation (EC) No 1907/2006
3. Substances restricted under Annex XVII of the REACH Regulation (EC) No 1907/2006
4. SCIP database established under the EU Waste Framework Directive 2008/98/EC (WFD).
5. persistent organic pollutants (POP)Regulation (EU) 2019/1021
6. Sweden’s Chemical Tax Act (2016:1067) (ECTA)
7. Chemicals Prohibition Ordinance – ChemVerbotsV
8. Medical Devices Regulation (EU) 2017/745 (“MDR”)
9. Substances classified under the battery regulation
10. Substances restricted under the Packaging Directive
11. Biocidal Products Regulation (BPR, Regulation (EU) 528/2012)
12. Cosmetics Regulation (EC) No 1223/2009
13. Toxic Substances Control Act of 1976 "TSCA" (Sec. 6(h))
14. Toxic Substances Control Act of 1976 "TSCA" (Sec. 5 (a)(2)
15. California Proposition 65 
16. PFAS in Maine in USA
17. Critical Raw Material Act
18. Repairability and Durability Index
19. Conflict Minerals Regulation
20. Supply Chain Act (Lieferkettengesetz)
21. Carbon footprint
22. Recycled content
23. PFAS Reporting under TSCA Section 8(a)(7)

Advantages of ComplyDoC

• All forms are prepared in digital format and stored in cloud
• Access from everywhere
• Secured with specific password for each user
• Customized solutions
• SQL Database
• Can be installed onsite, if requested
• Automatic submission of SCIP service
• PFAS Reporting to EPA
• Integration mit CDX for PFAS Reporting

In addition, we educate your suppliers to engage them in your sustainability and product compliance process.

Order please your Demo now.