Pharmaceuticals Information

30/09/2023

https://pharmaceuticalsindex.com/trend-analysis-2/

Follow OBJECTIVE To provide the guidelines for compilation of data for process parameters, assay values for actives to establish that Process performs according to design and is under control. Trend analysis data can be used to apply reduced testing in non-regulatory specifications after having esta...

30/09/2023

https://pharmaceuticalsindex.com/sop-for-quality-management-system-review/

Follow OBJECTIVE To review the Quality Management System implementation status and to plan for resolving any outstanding issue and for closing the gaps. SCOPE This SOP is applicable for holding Quality Management Review meeting system in (Company Name). RESPONSIBILITY 1. Team members of concerned de...

25/03/2023

https://pharmaceuticalsindex.com/pharmaceutical-companies-in-moldova/

Follow Alpen Pharma Group in Moldova E-mail: [email protected] Web: https://alpenpharma.md/ Address: Office Alpen Pharma in Moldova 10 Office, 40, S.Lazo Str., MD- 2004, Chisinau Balkan Pharmaceuticals in Moldova Web: https://balkanpharmaceuticals.com/ Address: Office Balkan Pharmaceutic...

25/03/2023

https://pharmaceuticalsindex.com/top-10-pharmaceutical-companies-in-australia/

Follow Below is the best list of 20 pharmaceutical companies in Australia; 1. Advanz Pharma (Australia) Advanz Pharma is a specialty pharmaceutical company with a strategic focus on complex medicines in Australia and Europe that is committed to improving the lives of patients by enhancing the critic...

25/03/2023

https://pharmaceuticalsindex.com/sop-for-retest-of-raw-materials/

Follow Objective To provide a written procedure for re-testing of raw materials. Scope This SOP shall be applicable for Quality Control and Quality Assurance Departments. Associated Documents: 1 Quality Assurance Report of Materials 2 Sampling Procedure for Raw Materials 3 Handling and Disposition o...

25/03/2023

https://pharmaceuticalsindex.com/pharmaceutical-companies-in-saudi-arabia/

Follow ABBOTT SAUDI ARABIA TRADING LLC. P.O.Box. 16082 Riyadh, 11464, Saudi Arabia AbbVie Biopharmaceuticals GmbH Abraj Attawuneyyah, North Tower, 16th Floor, P.O. Box 9710, Riyadh 11423, Kingdom of Saudi Arabia AcedrA Pharmaceutical Company Head Office: Al Riyadh, Platinum Centre, Az Zahra, Riyadh....

25/03/2023

https://pharmaceuticalsindex.com/top-10-pharmaceutical-companies-in-bangladesh/

Follow 1. Square Pharmaceuticals Ltd. Address & Location: SQUARE Centre 48, Mohakhali C/A Dhaka 1212, Bangladesh Website Name: https://www.squarepharma.com.bd/ Phone Number : +88-02-9859007 +88-02-8833047-56 Email Name: N/A Total Value (Cr. Taka): 1,511.53 Market Share (100): 18.78 Growth (%): 22.03...

25/03/2023

https://pharmaceuticalsindex.com/what-are-semi-solids/

Follow These products have semisolid consistency and applied to skin or mucous membranes for therapeutic orprotective action or cosmetic purpose. The following preparations belong to semisolid dosage products:creams, ointments, gel and pastes having viscous consistency. Definitions: Ointment: An oin...

25/03/2023

https://pharmaceuticalsindex.com/top-10-biotech-companies-in-scotland/

Follow Scotland is the UK’s second-most populous country, boasting picturesque scenery, a rich history, and a strong focus on sustainability. There is a diverse range of biotech startups in the region, with specialists in cell therapy, antimicrobials, industrial biotech, and more. 01. Amphista The...

20/03/2023

https://pharmaceuticalsindex.com/gmp-in-pharmaceuticals/

Follow Mohammad Abdul Motalib Momin: GMP refers to the Good Manufacturing Practices promoted by the WHO GMP Guidelines, implemented by the pharmaceutical manufacturers and monitored by the regulations promulgated by the Drug Regulatory Authorities (DRA); the document was published in 1975. The GMP r...

20/03/2023

https://pharmaceuticalsindex.com/performance-qualification/

Follow Performance Qualification (PQ) performed after successful completion of the Installation and Operational Qualifications ex*****on, for those critical systems or processes requiring PQ that should be validated to provide assurance of process repeatability. One of the purposes of PQ is to test....

20/03/2023

https://pharmaceuticalsindex.com/line-clearance-checklist-for-secondary-packaging-area/

Follow 1 Ensure that product containers, materials, status labels, BPR of previous process operation are removed. 2 Ensure that area is cleaned as per the cleaning procedure and records are updated. 3 Ensure that temperature, relative humidity and differential pressure of the area is suitable for di...

19/03/2023

https://pharmaceuticalsindex.com/

An online pharmaceuticals directory and gudeline.

19/03/2023

https://pharmaceuticalsindex.com/category/guideline/

Pharmaceutical Guideline

19/03/2023

https://pharmaceuticalsindex.com/fault-tree-analysis/

Follow Fault Tree Analysis (FTA) Description: Fault tree analysis is a deductive technique that assumes failure of the functionality of a product or process. From the failure of the functionality, the process looks at possible causes and links them down (in the form of a tree of fault modes) to the....

19/03/2023

https://pharmaceuticalsindex.com/general-considerations-for-process-validation/

Follow In all stages of the product lifecycle, good project management and good archiving that capture scientific knowledge will make the process validation program more effective and efficient. The following practices should ensure uniform collection and assessment of information about the process....

19/03/2023

https://pharmaceuticalsindex.com/quality-risk-management/

Follow Risk management principles are effectively utilized in many areas of business and government including finance, insurance, occupational safety, public health, pharmacovigilance, and by agencies regulating these industries. Although there are some examples of the use of quality risk management...

19/03/2023

https://pharmaceuticalsindex.com/cleaning-validation-handbook/

Follow The discipline of cleaning validation is as individual as process validation, but the methods, techniques, and risks are almost identical in all kinds of pharmaceutical manufacture. Process understanding is the magic term when assessing what must be done and the effort to be put into the docu...

19/03/2023

https://pharmaceuticalsindex.com/cleaning-validation-guideline/

Follow The subject of cleaning validation in active pharmaceutical ingredient manufacturing plants has continued to receive a large amount of attention from regulators, companies and customers alike. This guidance document has been updated by the APIC Cleaning Validation Task Force on behalf of the....

19/03/2023

https://pharmaceuticalsindex.com/alcoa/

Follow ALCOA principle to maintain data integrity: The ALCOA stands for A Attributable : Date should clearly state who performed the action and when? Data should be imputable implies that all collected information must-have info on WHO collected the info, who acted, and once the action was performed...

18/03/2023

https://pharmaceuticalsindex.com/pfizer-agrees-to-revise-eu-covid-vaccine-contract/

Follow Pfizer Inc agreed to extend its COVID-19 vaccine contract from 2023 to 2026 with the European Union, the Financial Times reported on Tuesday, citing people with knowledge of the matter. The drugmaker has offered to cut the number of doses being supplied by 40 per cent and delay delivery of th...

18/03/2023

https://pharmaceuticalsindex.com/fda-approves-pfizers-nasal-spray-for-migraine/
FDA approves Pfizer’s nasal spray for migraine

18/03/2023

https://pharmaceuticalsindex.com/installation-qualification/

Follow The data collected during the Installation Qualification can be packaged and summarized either individually or as part of an IQ/OQ/PQ package for presentation, review, and approval. The Installation Qualification Protocol provides a systematic method to check the system/equipment static attri...

18/03/2023

https://pharmaceuticalsindex.com/preparation-for-gmp-audit/

Follow GMP audit of any pharmaceutical industry is very important and crucial in its business. Therefore, before the audit, the preparation of the audit must be done properly. We can plan any GMP audit in the following ways: 1. Documents reviewed: A list of all documents related to the audit should....

19/05/2020

যেভাবে সপরিবারে করোনামুক্ত হলেন জানালেন বিটিভির মহাপরিচালক স্ত্রী-কন্যাসহ করোনামুক্ত হলেন বাংলাদেশ টেলিভিশনে...

15/05/2020

ঈদে ড. মাহফুজুর রহমানের একক সঙ্গীতানুষ্ঠান আসন্ন ঈদুল ফিতরে একক সঙ্গীতানুষ্ঠান নিয়ে হাজির হচ্ছেন এটিএন বাংলার চ....

15/05/2020

নিলাম বাতিল করলেন আশরাফুল বাংলাদেশ জাতীয় ক্রিকেট দলের সাবেক অধিনায়ক মোহাম্মাদ আশরাফুলের ব্যাট নিলামে উঠছে না। .....

15/05/2020

যুক্তরাষ্ট্রে করোনায় প্রাণ হারালেন আরও এক বাংলাদেশি করোনাভাইরাসে চিকিৎসারত অবস্থায় ১৩ মে বুধবার মারা গেলেন নিউ...

15/05/2020

রিক্সাচালক সেই বৃদ্ধ বর গ্রেফতার কিশোরীকে বিয়ে করা সেই বৃদ্ধ বর রিক্সাচালক সামছুল হককে গ্রেফতার করেছে কুমিল্লা.....