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Download CPOB 2018: Pedoman Cara Pembuatan Obat yang Baik


How to Download CPOB 2018 and Why You Should Do It




If you are involved in the drug manufacturing industry in Indonesia, you may have heard of CPOB 2018. CPOB stands for Cara Pembuatan Obat yang Baik, which means Good Manufacturing Practices for Drugs and Drug Ingredients. CPOB 2018 is the latest version of the guideline that regulates the quality standards for drug manufacturing in Indonesia. In this article, we will explain what CPOB 2018 is, what are the benefits of using it, how to download it from the official sources, and how to use it as a reference for your drug manufacturing activities.




download cpob 2018



What is CPOB 2018 and What are the Benefits of Using It




CPOB 2018 is the latest guideline for good manufacturing practices of drugs and drug ingredients in Indonesia




CPOB 2018 is a document that contains the principles, requirements, and recommendations for good manufacturing practices of drugs and drug ingredients in Indonesia. It was issued by the National Agency of Drug and Food Control (BPOM) in December 2018, based on the latest scientific and technological developments in the field of drug manufacturing. CPOB 2018 covers various aspects of drug manufacturing, such as quality system, personnel, premises and facilities, equipment, production, quality control, complaints and recalls, documentation, contract manufacturing and analysis, qualification and validation, etc. CPOB 2018 also includes several annexes that provide specific guidance for certain types of products, such as sterile products, blood products, medicinal gases, clinical trial products, computerized systems, etc.


CPOB 2018 ensures the quality, safety, and efficacy of drugs and drug ingredients




The main purpose of CPOB 2018 is to ensure that drugs and drug ingredients are produced consistently and controlled according to the quality standards that have been established. By following CPOB 2018, drug manufacturers can minimize the risks of producing substandard or defective products that may harm the consumers or patients. Moreover, by complying with CPOB 2018, drug manufacturers can also demonstrate their commitment to quality assurance and continuous improvement. This can enhance their reputation and competitiveness in the market.


CPOB 2018 is mandatory for all drug and drug ingredient manufacturers and facilities in Indonesia




According to the regulation of BPOM No. 34 Year 2018, CPOB 2018 is mandatory for all drug and drug ingredient manufacturers and facilities in Indonesia. This means that they have to obtain a certificate of compliance with CPOB 2018 from BPOM before they can operate or distribute their products. The certificate is valid for five years and can be renewed upon re-inspection by BPOM. Failure to comply with CPOB 2018 may result in sanctions such as warning letters, suspension or revocation of licenses, fines, or even criminal charges.


<h2 You should avoid downloading CPOB 2018 from unofficial or unverified sources as they may contain errors or viruses




Some websites may claim to offer CPOB 2018 for free or for a low price, but you should be careful and avoid them. These websites may not have the authorization or permission from BPOM to distribute CPOB 2018. They may also have modified or corrupted the original document, which can lead to misinformation or confusion. Worse, they may have infected the file with malware or viruses that can harm your computer or device. Therefore, you should always download CPOB 2018 from the official sources or from the sources that you trust.


How to Use CPOB 2018 as a Reference for Your Drug Manufacturing Activities




You should read and understand the contents of CPOB 2018 thoroughly before applying it to your processes




Before you start using CPOB 2018 as a reference for your drug manufacturing activities, you should read and understand the contents of the document thoroughly. You should familiarize yourself with the principles, requirements, and recommendations of CPOB 2018 and how they apply to your specific products and processes. You should also pay attention to the annexes that provide specific guidance for certain types of products, such as sterile products, blood products, medicinal gases, clinical trial products, computerized systems, etc. You should also consult with your quality assurance team, your technical experts, or your external consultants if you have any questions or doubts about CPOB 2018.


You should follow the requirements and recommendations of CPOB 2018 in every aspect of your drug manufacturing activities




Once you have understood the contents of CPOB 2018, you should follow them in every aspect of your drug manufacturing activities. You should implement a quality system that is based on CPOB 2018 standards and that covers all the stages of drug manufacturing, from raw materials to finished products. You should also ensure that your personnel are trained and qualified to perform their tasks according to CPOB 2018. You should also design and maintain your premises and facilities, your equipment, your production processes, and your quality control procedures in accordance with CPOB 2018. You should also document and record all your activities and results in a clear and accurate manner as required by CPOB 2018.


You should monitor and evaluate the effectiveness of your quality system based on CPOB 2018 standards




Following CPOB 2018 is not a one-time activity, but a continuous process of improvement. You should monitor and evaluate the effectiveness of your quality system based on CPOB 2018 standards on a regular basis. You should conduct internal audits and self-inspections to check whether you are complying with CPOB 2018 and whether there are any gaps or weaknesses in your system. You should also review and update your quality system whenever there are any changes in your products, processes, regulations, or customer expectations. You should also implement corrective and preventive actions whenever you find any non-conformities or deviations from CPOB 2018.


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Conclusion




CPOB 2018 is the latest guideline for good manufacturing practices of drugs and drug ingredients in Indonesia. It ensures the quality, safety, and efficacy of drugs and drug ingredients. It is mandatory for all drug and drug ingredient manufacturers and facilities in Indonesia. You can download CPOB 2018 from the official website of BPOM or from other reliable sources such as academic websites or online libraries. You should avoid downloading CPOB 2018 from unofficial or unverified sources as they may contain errors or viruses. You should read and understand the contents of CPOB 2018 thoroughly before applying it to your processes. You should follow the requirements and recommendations of CPOB 2018 in every aspect of your drug manufacturing activities. You should monitor and evaluate the effectiveness of your quality system based on CPOB 2018 standards.


FAQs




  • What is the difference between CPOB 2018 and previous versions of CPOB?



CPOB 2018 is the latest version of CPOB that was issued by BPOM in December 2018. It replaces the previous versions of CPOB that were issued in 2006 and 2009. CPOB 2018 incorporates the latest scientific and technological developments in the field of drug manufacturing. It also aligns with the international standards such as WHO GMP, PIC/S GMP, ICH Q7, etc.


  • How can I obtain a certificate of compliance with CPOB 2018 from BPOM?



To obtain a certificate of To obtain a certificate of compliance with CPOB 2018 from BPOM, you have to submit an application form and the required documents to the BPOM office in your region. You also have to pay the application fee and the inspection fee. BPOM will then conduct an inspection of your facility and your quality system based on CPOB 2018 standards. If you pass the inspection, BPOM will issue you a certificate of compliance with CPOB 2018 that is valid for five years. You


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