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Dr Reddy's board gives nod to induct third generation leadership into the company:

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Dr Reddy's board gives nod to induct third generation leadership into the company: Dr Reddy's Laboratories board has given green signal to induct Akhil Ravi, the son-in-law of GV Prasad, Co-Chairman, and CEO - of Dr Reddy's into the company management. Drug maker Dr Reddy’s Laboratories board has given green signal to induct Akhil Ravi, son-in-law of GV Prasad, co-Chairman and CEO of the company into the management. The decision was taken at the company's board meeting in October and was notified on Wednesday. Akhil Ravi represents the third generation of family leadership of Dr.Reddy's, founded by late K Anji Reddy. The company is now jointly run by Anji Reddy's son-in-law GV Prasad and son Satish Reddy, 50. The promoters hold 27.66 percent stake in the company. The drug maker ended with sales of little over Rs 14,000 crore in FY17. Akhil Ravi, who will be joining the company in a mid-senior management role as Director of Business Development a...
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AIR VELOCITY MEASUREMENT

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AIR VELOCITY MEASUREMENT Purpose: To provide a procedure to measure for airflow velocity and uniformity of velocity and supply airflow rate in clean room and clean zone. Scope: Applicable to all Air Handling Units system, Forced Air Ventilation system, Laminar Air Flow system(Unidirectional airflow system), Dynamic pass boxes, Garment Cubicles, Air showers, Air duct, Non unidirectional airflow installation(Diffuser, Grills, Risers). Responsibility: All HVAC Engineers. Definition: Uniformity of air flow: Unidirectional air flow pattern in which the point-to-point readings of velocities are within the defined percentage of the average airflow velocity. Unidirectional airflow: Controlled air flow through entire cross section of clean zone with steady velocity and approximately parallel streamlines. Non-Unidirectional airflow: Air distribution where the supply air entering the clean zone mixes with the internal air by means of induction. Laminar A...
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Pharma forum 2018(1)

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Pharma Forum 2018 11.     What do you mean by re-validation?  A repeat of the process validation to provide an assurance that changes in the  process/equipments introduced in accordance with change control procedures do not  adversely affect process characteristics & product quality.  22.     What do you mean by “worst case”?  A condition or set of conditions encompassing upper and lower processing limit and  circumstances, within standard operating procedures, which poses the greatest chance of  product or process failure when compared to ideal conditions. Such conditions do not  necessarily induce product or process failure.  33.     What do you mean by “performance qualification”?  The performance qualification documents describes the procedures for demonstrating that a  system / piece of equipment can consistently perform & meet required specifi...
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