Gujarat

In 2014, a Core Committee was constituted under the Chairmanship of Dr. VM Katoch by the Indian Health Ministry to revise National List of Essential Medicines (NLEM), 2011. In the process of revision of NLEM, several consultations were held across the country with experts from different domains.

Ajanta Pharma Ltd, a specialty pharmaceutical company engagi development, manufacture and marketing of quality finished dosaj in domestic and international markets, is looking for suita candidates for its Formulation facility at Dahej, Bharuch, Gujarat

Post : QC Officer/Executive (HPLC, GC, Micro LIMS)

Shri. Satsangi Saket Dham “Ram Ashram” Trust came into existence in 11th April 2001.  Managed by Shri. Satsangi Saket Dham “Ram Ashram”,  Shri. Satsangi Saket Dham is conceived as the educational township to house and nurture all sorts of institutions offering value added professional, internationally competitive and recognized programs on one hand, and on another hand institutions of primary and secondary education with sound foundations of learning and enculturation of orient values essentially Indian in spirit and heritage.

Post : Faculty

Leading Pharma Company- Nextus

Post: Area Manager

Winston HR Services is a HRD division launched by HR professional providing manpower recruitment & staffing services to Pharma, Chemical, Dyes, IT, Plastic, Engineering, Textile, Retail, Telecom, electrical & many more industries.

Post: Regulatory Affairs - 03 Posts

Application are invited for the following posts of the various posts para medical staff in BSF:

Post: ASI (Pharmacist- Qualified) (Group-C Post)

Envision Scientific is a company involved in research, development and manufacturing of innovative products and methods for treatment of cardiovascular disease. Envision Scientific is a company pioneering in the development of Nanotechnology based applications for delivery. Envision Scientific has developed a novel polymer free nanocarrier based drug delivery system in its R&D Lab.

Post : Executive/Sr. Executive - Purchase 1 Post

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ABOUT AUTHORS
Suleman S. khoja ¹, Sohil S khoja ¹,Parthkumar H chauhan ²,Farhad S Khoja
¹Resource person in pharmaceutical quality assurance ,VAPI, Gujarat.
²Resource person in quality assurance ,NAVSARI, Gujarat.
³Registered Pharmacist ,VAPI, Gujarat.
premukhoja@gmail.com

ABSTRACT
A review on USFDA observation and finding while inspection of Pharmaceutical the present review provide some important , Significant observation and measure of compliance.USFDA is an regulatory body governing health products which are made ( in or  outside USA) and marketed in united States of America. Significant deviation from cGMP and Significant violation from cGMP for both API Facility and formulations .strictly compliance requirements under 21 Code of federal regulations (CFR). FDA observation includes but not limited to this. If not cleaned and maintained equipment at appropriate intervals to prevent contamination that would alter the Safety, Identity, Strength, Purity and Quality of drug product (SISPQ) ,violation under [ 21 CFR & 211.67 (a) ]. Data integrity is main issue Raised in most FDA warning letter. Corrective action and plan. Level of control must be raised from raw material, packaging material (Accurate, Legible, Contamptarious, Original, Attributable (ALCOA)) in process, finished dosage form, Maintain log book properly. Guidelines for Out of specification(OOS ) and out of trends(OOT)  must be follow if any required.