As you know in pharmaceutical industry there are various departments like Production, Quality Control, Quality Assurance, Engineering, Technology Transfer, Warehouse, Research and development and Human resource Department etc. Refer Production Personnel Responsibilities : https://pharmaceuticalupdates.com/2020/06/23/responsibilities-of-production-personnel-in-pharmaceuticals/ Refer Quality Assurance Personnel Responsibilities : https://pharmaceuticalupdates.com/2019/01/26/responsibility-of-quality-assurance-personnel-or-quality-unit-in-pharmaceuticals/ Refer Quality Control Personnel Responsibilities : https://pharmaceuticalupdates.com/2020/05/02/responsibilities-of-quality-control-personnel/ Warehouse or Stores are the department in … Continue reading Warehouse Personnel Responsibilities in Pharmaceuticals →

Each departments have their own responsibilities in Pharmaceutical and based up on the job responsibility every body has to work. Job responsibility shall be assigned to the persons based upon Educational Qualification and Experience and according to the job responsibility every body has to take Standard Operating Procedure (SOP) Training. Following are the job responsibilities … Continue reading Production Personnel Responsibilities in Pharmaceuticals →

Below are the general procedure for good controls and practices for Packaging Activities in Pharmaceuticals and the persons working in packing department should follow the procedure for better control and compliance. Every person should follow personnel entry and exit procedure for entry and exit in Packing Area as per SOP (Standard Operating Procedure). For SOP … Continue reading Good Control and Practices in Packaging →

Training plays an important role in any industry and it gives a clear understanding about the roles and responsibilities of a person working in an organization. There are different types of Training which are as follows (1)  Induction Training (2)  On Job Training (3)  Self Reading Training(4)  Class Room Training(5)  External Training (6)  Incidental Training (7)  Refresher Training  Induction … Continue reading Different Types of Training in Pharmaceuticals →

It is our responsibility to follow the below mentioned principles wherever possible and the government is also using these principles as the basis of discussions with businesses, unions, local government and many other stakeholders, to agree how the principles should apply in different settings to make them safer. All of us, as customers, visitors, employees … Continue reading During COVID-19 how to stay safe outside your Home →

These temporary good manufacturing practice (GMP) flexibilities will be allowed to address the current exceptional circumstances. These flexibilities will enable manufacturers to release additional quality system capacity for to focus on ensuring continuity of supply using quality risk management principles Manufacture and importation Where appropriate based on risk, testing of raw materials may be limited … Continue reading Exceptional GMP Flexibilities for Medicines Manufacturers during the corona virus (COVID-19) →

Due to the COVID-19 pandemic, remote working has increased and some organizations have advised that their processes for approving paper documents with wet ink signatures are no longer achievable. This guidance is to enable organizations to consider alternative methods whilst maintaining basic control of documents. The guidance is for organizations involved in the pharmaceutical lifecycle … Continue reading During (COVID-19) Epidemic the Approval of documents when working from home →

Medicines and Health care products Regulatory agency (MHRA) are allowing alternative courses of actions for manufacturing or Quality control laboratory equipments or instruments during the outbreak. During the corona virus pandemic it may not be possible for service personnel or external engineering support to operate as normal hence the following options are available to manufacturers … Continue reading During COVID-19 Epidemic the Unusual Flexibilities for Maintenance and Calibration Activities →