Category Archives: News Updates

Global Challenges for Indian Pharmaceutical Industry

The Indian pharma industry is on a good growth path and is likely to be in the top 10 global markets by value by 2020. High burden of disease, good economic growth leading to higher disposable incomes, improvements in healthcare … Continue reading

Posted in Interview & Placement, News Updates, quality assurance, Steam Sterilizer, Validation | 1 Comment

Troubleshooting in pharmaceutical industry automation Vs Manual

New era of Indian Pharmaceutical industry is going to begin. Major regulatory pharmaceutical companies are under USFDA alert. Repeated/similar observation are reported against data integrity and GMP practices. Now a day’s process are dependent on the human being, however transition … Continue reading

Posted in News Updates | 2 Comments

Review and monitoring the sterility assurance level

One of the most critical operations in pharmaceutical manufacturing is the processing of sterile products. The production of sterile products, specifically the ones that cannot be terminally sterilized,involve complex and demanding processes to prevent the products’ contamination and require a … Continue reading

Posted in News Updates | 6 Comments

Clearing the Mystery of Dynamic Pass Box

Few facts about Dynamic Pass Box Through this blog we will be providing you the qualification and routine maintenance of dynamic pass boxes in your critical and non critical area.  As per the industrial practices some time we do more … Continue reading

Posted in News Updates | 3 Comments

Untouched area of Data Integrity in Pharmaceutical Industry

Now a days the topic “Data integrity and non compliance” is the hot topics. Lots of references available online that deals with the Data integrity issue. One of the major example am going to give today, that can be control by … Continue reading

Posted in audit, Drug regulatory and guidelines, News Updates | 1 Comment

Reason for Data Integrity in pharma industry

We know the available elements of ALCOA. We will discuss latter on the ALCOA topic. But currently we want to emphasis on the issue why we are getting this issues? Data integrity no only the problem of a specific organization, … Continue reading

Posted in Drug regulatory and guidelines, Interview & Placement, News Updates | 3 Comments

Complication in Pharma industry with stability issue and salary expectation in Indian scenario

Now a days the pattern of interview is very interesting in pharma industry. The main argument comes with following points, Expected designation  Experience  Expected salary  Expected Stability   As we know the vertical is different from organization to organization. Normally … Continue reading

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Paperless documentation in pharma..a steps towards next generations

1. Put a weight machine to measures paper waste in QA…to check how many paper we shredded per months.. May be tons off.. 2. Build awareness among the people by showing the data.. 3. Make a campaign to reduced the … Continue reading

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WEB Presentation

Web presentation is an innovative idea to share pharmaceutical Knowledge, following PPT’s are updated currently  1. QRM – On Quality Risk Management  2. Make your company presentation  3. A brief review on HVAC system http://www.slideshare.net/PalashDas10/slideshelf

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Major USFDA warning Letters observation from 2000

The United States Food and Drug Administration (FDA) defines a Warning Letter as “…a correspondence that notifies regulated industry about violations that FDA has documented during its inspections or investigations. Typically, a Warning Letter notifies a responsible individual or firm … Continue reading

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