Drug Regulatory Authority of Pakistan, Ministry of SRO 824(I)/2018 dated 26th June, 2018 regarding amendments in Schedule-I para 2(b) DRAP Act 2012: Medical Devices: Download: SROs: SRO 143(I)/2018 dated 7th Feb, 2018 regarding constitution of Medical Device Board: Medical Devices: Download: SROs: SRO 1571(I)/2019 - Notification of CDL for testing the quality, safety and performance ofContact Supplier

Fed govt puts sanitizer manufacturing under DRAP controlLAHORE: In a surprise move the federal government has put hand sanitizer manufacturing under the control of Drug Regulatory Authority of Pakistan (DRAP) and allowing controlling it as regulatedContact Supplier

DRAP Bans Unlicensed Companies From Making Hand SanitizersThe DRAP notification said that the decision was taken in the public interest, considering the health urgency and the need for quality hand sanitizers to save people from the coronavirus pandemicContact Supplier

FDA Registration and NDC Number for Hand SanitizerHand Sanitizer - Active Ingredients benzalkonium chloride, Alcohol (ethyl alcohol or ethanol, 60 to 95 percent), and isopropyl alcohol (70 to 913 percent) are still under FDA OTC Drug review and are eligible for marketing, manufacturers of hand sanitizers with these ingredients continue with FDA drug establishment registration renewal and drugContact Supplier

Hand Sanitizer (Instant, Clean & Soft) DRAP-Permission No Hand Sanitizer (Instant, Clean & Soft) DRAP-Permission No 1387720(Gel) Tested by PSQCA:Ref QCC-4(360)19-20 quantityContact Supplier

FDA Registration and NDC Number for Hand SanitizerHand Sanitizer - Active Ingredients benzalkonium chloride, Alcohol (ethyl alcohol or ethanol, 60 to 95 percent), and isopropyl alcohol (70 to 913 percent) are still under FDA OTC Drug review and are eligible for marketing, manufacturers of hand sanitizers with these ingredients continue with FDA drug establishment registration renewal and drugContact Supplier

Hand Sanitizer (Instant, Clean & Soft) DRAP-Permission No Hand Sanitizer (Instant, Clean & Soft) DRAP-Permission No 1387720(Gel) Tested by PSQCA:Ref QCC-4(360)19-20 quantityContact Supplier

Drug Regulatory Authority of Pakistan, Ministry of Deferred Applications of Hand Sanitizers: 10-04-2020: Defferd,hand,sanitizer: HOTC: Download: Letter: Rejected Applications of Hand Sanitizers: 10-04-2020: Rejected,hand,sanitizer: HOTC: Download: Letter: Letter of cases of sanitizers permitted in 76th meeting of EEC held on 10th April, 2020: 14-04-2020: permitted, sanitizer,76: HOTC: DownloadContact Supplier

FDA Registration and NDC Number for Hand SanitizerHand Sanitizer - Active Ingredients benzalkonium chloride, Alcohol (ethyl alcohol or ethanol, 60 to 95 percent), and isopropyl alcohol (70 to 913 percent) are still under FDA OTC Drug review and are eligible for marketing, manufacturers of hand sanitizers with these ingredients continue with FDA drug establishment registration renewal and drugContact Supplier

Drug Regulatory Authority of Pakistan, Ministry of SRO 824(I)/2018 dated 26th June, 2018 regarding amendments in Schedule-I para 2(b) DRAP Act 2012: Medical Devices: Download: SROs: SRO 143(I)/2018 dated 7th Feb, 2018 regarding constitution of Medical Device Board: Medical Devices: Download: SROs: SRO 1571(I)/2019 - Notification of CDL for testing the quality, safety and performance ofContact Supplier

Drug Regulatory Authority of Pakistan, Ministry of SRO 824(I)/2018 dated 26th June, 2018 regarding amendments in Schedule-I para 2(b) DRAP Act 2012: Medical Devices: Download: SROs: SRO 143(I)/2018 dated 7th Feb, 2018 regarding constitution of Medical Device Board: Medical Devices: Download: SROs: SRO 1571(I)/2019 - Notification of CDL for testing the quality, safety and performance ofContact Supplier

GOVERNMENT OF PAKISTAN Ministry of National Health of quality hand sanitizers during COVID-19pandemic, decided the following in the best public interest:-(I) The manufacturers having valid Drug Manufacturing License (DML) or valid Enlistment Certificates (Form-6) with topical or external preparations section may prepare hand-sanitizer with the below mentioned WHO recommended formulations onlyContact Supplier

Fed govt puts sanitizer manufacturing under DRAP controlLAHORE: In a surprise move the federal government has put hand sanitizer manufacturing under the control of Drug Regulatory Authority of Pakistan (DRAP) and allowing controlling it as regulatedContact Supplier

Hand Sanitizer (Instant, Clean & Soft) DRAP-Permission No Hand Sanitizer (Instant, Clean & Soft) DRAP-Permission No 1387720(Gel) Tested by PSQCA:Ref QCC-4(360)19-20 quantityContact Supplier

Drug Regulatory Authority of Pakistan, Ministry of Deferred Applications of Hand Sanitizers: 10-04-2020: Defferd,hand,sanitizer: HOTC: Download: Letter: Rejected Applications of Hand Sanitizers: 10-04-2020: Rejected,hand,sanitizer: HOTC: Download: Letter: Letter of cases of sanitizers permitted in 76th meeting of EEC held on 10th April, 2020: 14-04-2020: permitted, sanitizer,76: HOTC: DownloadContact Supplier

DRAP Bans Unlicensed Companies From Making Hand SanitizersThe DRAP notification said that the decision was taken in the public interest, considering the health urgency and the need for quality hand sanitizers to save people from the coronavirus pandemicContact Supplier

FDA Registration and NDC Number for Hand SanitizerHand Sanitizer - Active Ingredients benzalkonium chloride, Alcohol (ethyl alcohol or ethanol, 60 to 95 percent), and isopropyl alcohol (70 to 913 percent) are still under FDA OTC Drug review and are eligible for marketing, manufacturers of hand sanitizers with these ingredients continue with FDA drug establishment registration renewal and drugContact Supplier

Drug Regulatory Authority of Pakistan, Ministry of Deferred Applications of Hand Sanitizers [10 Apr, 2020] Rejected Applications of Hand Sanitizers [10 Apr, DRAP,as part of its special campaigns against spurious drugs in the country, has ensured testing of 1,71,375 samples at its laboratories during two years and nine monthsContact Supplier

Drug Regulatory Authority of Pakistan, Ministry of Deferred Applications of Hand Sanitizers [10 Apr, 2020] Rejected Applications of Hand Sanitizers [10 Apr, DRAP,as part of its special campaigns against spurious drugs in the country, has ensured testing of 1,71,375 samples at its laboratories during two years and nine monthsContact Supplier

DRAP Bans Unlicensed Companies From Making Hand SanitizersThe DRAP notification said that the decision was taken in the public interest, considering the health urgency and the need for quality hand sanitizers to save people from the coronavirus pandemicContact Supplier

FDA Registration and NDC Number for Hand SanitizerHand Sanitizer - Active Ingredients benzalkonium chloride, Alcohol (ethyl alcohol or ethanol, 60 to 95 percent), and isopropyl alcohol (70 to 913 percent) are still under FDA OTC Drug review and are eligible for marketing, manufacturers of hand sanitizers with these ingredients continue with FDA drug establishment registration renewal and drugContact Supplier

Drug Regulatory Authority of Pakistan, Ministry of Deferred Applications of Hand Sanitizers: 10-04-2020: Defferd,hand,sanitizer: HOTC: Download: Letter: Rejected Applications of Hand Sanitizers: 10-04-2020: Rejected,hand,sanitizer: HOTC: Download: Letter: Letter of cases of sanitizers permitted in 76th meeting of EEC held on 10th April, 2020: 14-04-2020: permitted, sanitizer,76: HOTC: DownloadContact Supplier

Drug Regulatory Authority of Pakistan, Ministry of Deferred Applications of Hand Sanitizers [10 Apr, 2020] Rejected Applications of Hand Sanitizers [10 Apr, DRAP,as part of its special campaigns against spurious drugs in the country, has ensured testing of 1,71,375 samples at its laboratories during two years and nine monthsContact Supplier

Fed govt puts sanitizer manufacturing under DRAP controlLAHORE: In a surprise move the federal government has put hand sanitizer manufacturing under the control of Drug Regulatory Authority of Pakistan (DRAP) and allowing controlling it as regulatedContact Supplier