Drug Regulatory Authority Of Pakistan Jobs have been announced for the posts of Director (Budget and Accountant), Director (Legal Affairs Division), Director (Technical Carde), Assistant Director (Legal Affairs Division), Assistant Director (Technical Carde), Stenotypist, Data Entry Operator, and Electrician.
Official advertisement, eligibility criteria, the online application process, and the last date to apply for Drug Regulatory Authority Of Pakistan Jobs have been given below.
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| Designation Director (Budget and Accountant), Director (Legal Affairs Division) | Age Limit 18-47 | Who Can Apply Male, Female |
| Salary Offered Pkr. 100,000 | Job Location Islamabad | Category Government Jobs |
| Date Posted 15 July 2023 | Job Type Permanent Basis | Last Date To Apply 30 July 2023 |
Drug Regulatory Authority Of Pakistan Jobs 2023
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Qualification Required for Drug Regulatory Authority Of Pakistan Jobs
The minimum qualification for these Jobs is a P.h.D/LLB/Master’s degree etc according to a job from a Government or private certified institution.
Experience Required For Drug Regulatory Authority Of Pakistan Jobs
Interested candidates must have at least 10 years of experience in some jobs in the relevant field from a renowned institution.
Experienced candidates would be preferred over fresh ones. Although fresh candidates can also apply for these jobs.
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Drug Regulatory Authority Of Pakistan Jobs Online Application Form
The official online application process for these jobs is given in the following image. Read it carefully before applying for these jobs.
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Drug Regulatory Authority Of Pakistan Jobs 2023 Official Advertisement
The following is the official advertisement for these jobs. You can also visit the DRAP Jobs Official website to see details of these jobs by clicking here.
DRAP Helpline Number
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Official Website: https://www.dra.gov.pk/
Address: Telecom Foundation Complex, Mauve Area, G-9/4, Islamabad, Pakistan
Phone: +92-51-9107313
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DRAP Jobs FAQs
What is the last date to apply for the Drug Regulatory Authority Of Pakistan Jobs?
The last date to apply for Drug Regulatory Authority Of Pakistan Jobs is 30 July 2023.
Qualifications Required for Drug Regulatory Authority Of Pakistan Jobs?
The required Qualification for these jobs is a P.h.D/LLB/Master’s Degree from an HEC-recognized institution.
What is the Basic Pay Scale of the Drug Regulatory Authority Of Pakistan Jobs?
The basic pay scale of the Drug Regulatory Authority Of Pakistan Jobs Is BPS-12.
What is the Contact Number Drug Regulatory Authority Of Pakistan Jobs?
DRAP’s Contact Number is as follows
Official Website: https://www.dra.gov.pk/
Address: Telecom Foundation Complex, Mauve Area, G-9/4, Islamabad, Pakistan
Phone: +92-51-9107313
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Drug Regulatory Authority of Pakistan
The Drug Regulatory Authority of Pakistan (DRAP) plays a crucial role in regulating and overseeing various therapeutic goods to ensure public health and safety.
Let’s discuss in detail the responsibilities and functions of DRAP:
- Regulatory Oversight: DRAP is responsible for regulating and overseeing a wide range of therapeutic goods, including pharmaceutical and biological drugs for both human and veterinary use, medical devices, medical cosmetics, and various health & OTC (non-drug) products, which are commonly known as alternative medicines. These alternative medicines include Ayurvedic, Chinese, Unani, Homeopathy, Nutritional products, and Food supplements for humans and animals.
- Legislation Enforcement: The DRAP Act of 2012 empowers the authority to effectively coordinate and enforce The Drugs Act, 1976 (XXXI of 1976). This ensures that all therapeutic goods in Pakistan adhere to the relevant regulations and standards, fostering a harmonious inter-provincial trade and commerce environment.
- Quality, Safety, and Efficacy Assurance: DRAP’s primary objective is to ensure that therapeutic goods approved and available in the market meet prescribed standards of quality, safety, and efficacy. This is to safeguard public health and ensure that consumers receive products that are effective and safe for their intended use.
- Registration and Marketing Authorization: Before any therapeutic good can be marketed and sold in Pakistan, it must go through a registration and marketing authorization process with DRAP. This involves a comprehensive evaluation of the product’s quality, safety, and efficacy data, including information from clinical trials and laboratory testing.
- Vigilance and Pharmacovigilance: DRAP is responsible for monitoring and maintaining vigilance over the safety of therapeutic goods in the market. This includes collecting and analyzing adverse event reports and taking appropriate actions to mitigate any identified risks to public health.
- Market Surveillance and Control: DRAP conducts regular market surveillance activities to ensure that the products available in the market comply with the approved specifications and standards. This involves inspecting manufacturing facilities, distribution centers, and retail outlets to check for compliance with regulations.
- Licensing Establishments: DRAP issues licenses to establishments involved in the manufacturing, import, export, distribution, and sale of therapeutic goods. These licenses are subject to compliance with relevant regulations and standards.
- Regulatory Inspection: The authority conducts inspections of manufacturing facilities, warehouses, and distribution centers to verify compliance with Good Manufacturing Practices (GMP) and Good Distribution Practices (GDP). These inspections aim to ensure the quality and safety of therapeutic goods.
- Laboratory Testing: DRAP operates its own testing laboratories to assess the quality and safety of therapeutic goods. The laboratories analyze samples of drugs and medical devices to verify their compliance with prescribed standards.
- Oversight of Clinical Trials: For new drugs and medical devices, DRAP oversees and evaluates clinical trials conducted in Pakistan. This process ensures that clinical trials are conducted ethically and with due consideration for the safety and well-being of trial participants.
- Lot Release of Biologicals: Biological drugs, which include vaccines and other biotechnologically derived products, undergo a lot of release processes to ensure their quality and safety before they are released for distribution and use.
Overall, the Drug Regulatory Authority of Pakistan plays a critical role in safeguarding public health by ensuring that all therapeutic goods in the market meet stringent quality, safety, and efficacy standards.
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Drug Regulatory Authority of Pakistan DRAP Jobs
The Drug Regulatory Authority of Pakistan (DRAP Jobs) plays a crucial role in regulating and ensuring the safety, quality, and efficacy of therapeutic goods in Pakistan.
Let’s discuss in detail the various regulatory functions performed by DRAP Jobs:
- Registration and Marketing Authorization of Therapeutic Goods: DRAP is responsible for the registration and marketing authorization of pharmaceutical and biological drugs, medical devices, medical cosmetics, and alternative medicines. Before a product can be introduced to the market, it must undergo a thorough evaluation by DRAP to ensure its compliance with established standards and guidelines. This process involves reviewing the product’s documentation, clinical data, manufacturing practices, and labeling information to determine its suitability for approval.
- Vigilance Activities: Once a therapeutic product is approved and available in the market, DRAP continues to monitor its safety and effectiveness through vigilance activities. This includes collecting and analyzing data on adverse drug reactions (ADRs) and other related events. If any safety concerns arise, DRAP takes appropriate actions, such as issuing safety alerts, recalls, or warnings, to protect public health.
- Market Surveillance and Control: DRAP conducts market surveillance to identify and address any issues related to therapeutic goods available in the market. This includes monitoring the quality, labeling, and packaging of products to ensure compliance with regulations. If substandard or counterfeit products are found, DRAP takes swift action to remove them from circulation and take legal actions against the offenders.
- Licensing Establishments: DRAP is responsible for licensing establishments involved in the production, import, and distribution of therapeutic goods. These establishments must meet specific criteria and adhere to Good Manufacturing Practices (GMP) to ensure the quality and safety of the products they handle. Regular inspections are carried out to ensure compliance with these standards.
- Regulatory Inspection of Facilities: To ensure that manufacturers, importers, and distributors of therapeutic goods meet the required quality and safety standards, DRAP conducts regulatory inspections of their facilities. These inspections assess the manufacturing processes, storage conditions, quality control measures, and adherence to regulatory guidelines.
- Laboratory Testing: DRAP operates accredited laboratories that conduct rigorous testing of therapeutic goods to verify their quality and safety. These tests include analyzing the composition, potency, purity, and stability of drugs and other medical products. Laboratory testing is an essential aspect of ensuring that products meet the prescribed standards.
- Oversight of Clinical Trials: For new pharmaceutical and biological drugs, DRAP provides oversight of clinical trials to safeguard the rights and safety of participants. The authority evaluates trial protocols, informed consent processes, and ethical considerations before granting approval for conducting clinical research.
- Pharmacovigilance: Pharmacovigilance is the process of monitoring, assessing, and managing the risks associated with therapeutic products after they are marketed. DRAP collects and analyzes data on adverse events and reactions to evaluate the safety profile of approved products continually.
- Lot Release of Biologicals: Biological products, such as vaccines and blood products, are subject to lot release by DRAP before distribution. This process involves evaluating samples from each batch to ensure their quality and safety before they reach the public.
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