Regulatory Guide
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Philippines DOH Guide for Me...
Philippines DOH Guide for Medical Device -> REGULATORY AGENCY Department of Health (DOH) REGULATIONS Manufacturers need to obtain a License to Operate (LTO) and a Certificate of Product Registration (CPR) from BFAD (Bureau of Food and Drugs).
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Philippines BPS Guide for En...
Philippines BPS Guide for Energy Efficiency -> REGULATORY AGENCY Bureau of Product Standards (BPS), Department of Trade and Industry (DTI) REGULATIONS Minimum Energy Performance Standards (MEPS) are required for certain products.
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Philippines BPS Guide for Sa...
Philippines BPS Guide for Safety Device - REGULATORY AGENCY Bureau of Product Standards (BPS), Department of Trade and Industry (DTI) REGULATIONS Manufacturers need to comply with mandatory requirements by obtaining the Philippine Standard (PS) Quali
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Philippines NTC Guide for R&...
Philippines NTC Guide for R&TTE Device -> REGULATORY AGENCY National Telecommunications Commission (NTC) REGULATIONS Terminal Equipment, or Customer Premises Equipment (CPE) and Radio Communications Equipment (RCE) require certification by NTC.
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Kazakhstan Medical Guide
Kazakhstan Medical Guide -> REGULATORY AGENCIES Control committee of medical and pharmaceutical activity, Pharmaceutical Control Division of Alma-Ata under the Ministry of Healthcare and Social Development of the Republic of Kazakhstan National Center
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Kazakhstan ECC Guide for Saf...
Kazakhstan ECC Guide for Safety Device -> REGULATORY AGENCY Eurasian Economic Commission REGULATIONS Technical regulations of the Customs Union "On safety of low-voltage equipment" (TP TC 004/2011) came into force on 15 February 2013.
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Kazakhstan TELSET Guide for ...
Kazakhstan TELSET Guide for R&TTE Device -> REGULATORY AGENCY “TELSET” Certification Body for Telecommunication REGULATIONS According to the Law of the Republic of Kazakhstan "About communication" the communication facilities realisation in Kazakhs
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Israel IMOH Guide for Medica...
Israel IMOH Guide for Medical Device -> REGULATORY AGENCY Israel’s Ministry of Health (IMOH) REGULATIONS All medical devices, including biologics, must be registered with IMOH. IMOH recognises US FDA certification and the EU CE Mark, and usually app
