• SRF Limited, a manufacturer of speciality chemicals are intending to manufacture propellants for metered dose inhalers at their Dahej Plant, Gujarat. . GMP Pharma consultants will be helping them in a comprehensive manner in establishing the facility

• GMP Pharma consultants did an audit of the facilities of ITC limited , Haridwar for their expansion into various products on 28th June 2015

• GMP Pharma consultants carried out GMP compliance audits at S Kant Healthcare , Vapi and R N Laboratories , Surat, Gujarat on 13th , 14th and 15th June 2015 on behalf of a European client

• GMP Pharma consultants carried out GMP compliance audits at Microlabs, Hosur , Tamil Nadu on 6th June 2015 on behalf of a European client

• GMP Pharma consultants carried out inspection of analysis of a certain product at Medopharm , Malur, Karnataka on 22nd and 23rd June 2015 on behalf of a European client

• GMP Pharma consultants audited CSPC Shiyao Yinhu Pharmaceuticals Limited, China , a sterile manufacturing facility for GMP compliance on behalf an European client on 14th and 15th May 2015.

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• GMP Pharma consultants audited Hebei Jiheng Pharmaceutical Company , China , an oral dosage manufacturing facility for GMP compliance on behalf an European client on 11th and 12th May 2015

• GMP Pharma consultants audited Maneesh Pharmaceuticals , Mumbai , India an oral dosage manufacturing facility for GMP compliance on behalf an European client on 10th April 2015.

• GMP Pharma consultants audited Maneesh exports , Mumbai , India an oral dosage manufacturing facility for GMP compliance on behalf an European client on 11th April 2015.

• GMP Pharma have got a contract from Civenti Pharma , Hyderabad to train all their employees on all aspects of cGMP.

• GMP Pharma have got a contract from Arunodaya Printers to establish quality systems in their factory .

• GMP Pharma consultants have successfully completed a 2 weeks tour of China where they audited several formulation companies on behalf of an European Clients.

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• GMP Pharma consultants audited Auctus Pharma at Vishakapatnam for compliance with USFDA requirements from an infrastructure as well as systems point of view over an 8 day period.

• GMP Pharma consultants are auditing various formulations plants, manufacturing oral dosage forms as well Injections in Shijiazhuang over a 15 day period starting from 24th December till 5th Dec. They are carrying out these audits on behalf of an European client.

• GMP Pharma consultants are conducting a series of training programmes on cGMP in Everest Organics, a leading API manufacturer.

• GMP Pharma consultants did a comprehensive audit of CELON Laboratories encompassing Infrastructure, QA, QC, Maintenance and Warehouse. This was spread over 3 days. As a sequel, GMP Pharma have contract to improve the quality systems.

• GMP Pharma are carrying out a series of training programmes on cGMP in Shasun Pharmaceuticals, Cuddalore and Pondicherry in vernacular covering operators and supervisors.

• GMP Pharma consultants have won a contract from Arunodaya Printers, manufacturers of Flexo films and pulp board cartons for improving their quality systems.

• GMP Pharma consultants completed a gap analysis of Arunodaya Printers, Apparel Park, Hyderabad for compliance with quality systems and submitted a report.

• TEVA Pharmaceuticals Pvt Limited have extended their contract with GMP Pharma. Our personnel have now been deputed to Goa, Pune and Haridwar.

• GMP Pharma consultants have got an assignment for document verification from TEVA, the large generics company, at one of their manufacturing sites. 10 of GMP Pharma personnel are working at the site.

• GMP Pharma consultants carried out a comprehensive training programme on sterile operations at Green Signal bio Pharma, Gummdipoondi, near Chennai.

• GMP Pharma consultants have been awarded a contract for designing a plant for manufacture of Diagnostics. The company is Nexogenix and is located ICICI knowledge park.

• GMP Pharma consultants audited an API manufacturer Covalent laboratories, Sangareddi, Hyderabad as per International GMP compliance.

• GMP Pharma have done documentation audits at Micro labs and Aurobindo Pharma - Formulations units as a service to a European client .

• GMP Pharma consultants have a contract to upgrade the documentation of Rx Homeo Pharma, USA.

• GMP Pharma conducted an awareness programme on Good Laboratory practices at SAPALA Organics, Nacharam, Hyderabad .

• GMP Pharma consultants have a contract to upgrade the documentation of Rx Homeo Pharma, USA.

• GMP Pharma conducted an awareness programme on Good Laboratory practices at SAPALA Organics, Nacharam, Hyderabad .

• Nosch labs Private Limited, Nagaram plant, which was inspected by EU regulators in November 2013, has been approved by the EU authorities. GMP Pharma consultants compliments them on their efforts. GMP Pharma consultants are proud to have been associated with the company in this process of compliance.

• GMP Pharma consultants carried out sampling of finished products as well verified documents of select products at Galentic, Navi Mumbai. Sirmaxo, Tarapore, Mumbai, Aurobindo Hyderabad and Micro labs, Bangalore on behalf of an European client.

• GMP Pharma consultants have been awarded a six month assignment for upgrading of GMP at Hygro Pharmatek, Vishakapatnam. Hygro Pharmatek are one of the oldest clients of GMP Pharma for the past 11 years.

• GMP Pharma helped Chowdhary and company, a manufacturing company dealing with mining chemicals, in the areas upgrading their GMP. They manufacture Talc and Calcium Carbonate and supply to various food, paint and Pharmaceutical industries.

• GMP Pharma consultants have carried out a GMP compliance audit of COVALENT laboratories, Sangareddi, Andhra Pradesh on behalf of ZIM Laboratories, Nagpur on 18^th September.

• GMP Pharma Consultants have carried out an introductory programme to the scientists of Daicel Chiral Technologies India Private Limited, ICICI Knowledge Park on 22^nd September.

• SIPRA laboratories, Hyderabad has entered into a contract with GMP Pharma Consultants for conducting a series of training programmes for all their personnel, for a period of six months.

• GMP Pharma Consultants have signed a contract with ZIM laboratories Limited, Nagpur for upgrading the company’s GMP. This contract is valid for a period of 1 year from September 2013.

• GMP Pharma consultants audited the following facilities as per WHO guidelines on 30^th July, 31^st July and 1^st August 2013 respectively on behalf of an European Client.
  • Sirmaxo Chemicals, Tarapore, manufacturer of topical preparations.
  • Galentic Pharma, Navi Mumbai, manufacturer of creams and ointments.
  • Ciron Drugs, Tarapore, manufacturer of sterile solids for injections.

• GMP Pharma consultants conducted a training programme on documentation and maintenance to managers and Executives of Hemmo Pharma Private Limited, Thurbe, Navi Mumbai on 12^th August 2013.

• GMP Pharma consultants conducted a training programme on ICH Q 7 to managers and Executives of Salicylates and Chemicals Private Limited, Hyderabad on 14^th August 2013.

• GMP Pharma consultants audited VIMTA laboratories Limited for Good laboratory compliance on 22^nd July 2013, on behalf an European client.

• GMP Pharma has started training new batches of Students in VIPER Narsapur and Vishnu College, Bhimavaram.

• GMP Pharma Consultants have audited 4 different manufacturing locations of CSPC Pharmaceutical (Shijiazhuang) Company Limited, Located at Shijiazhuang, China – 2 units manufacturing sterile powder for injections and 2 units manufacturing solid dosage forms on a third party basis for an European client. The audit was done over a period of six days.

• GMP Pharma have completed the task of giving a design in order to modify the existing AHU system at AET Laboratories – a multinational CRO company located in Andhra Pradesh.

• GMP Pharma Consultants picked up samples from Marck Biosciences on behalf of an international client located in Europe.

• GMP Pharma Consultants have been awarded two contracts for upgrading GMP in Ciron Drugs and Pharmaceuticals – one for their Tarapore plant and another for their Palghar plant.

• GMP Pharma Consultants have prepared product dossiers to be submitted to regulatory authorities in Tanzania. This has been done for an international client located in Europe.

• GMP Pharma Consultants audited Reyoung Pharmaceuticals located in Ye Yuan Country, Shandong Province, China. The dry powder injection facility was audited for compliance with cGMP norms. This audit was done on 28th & 29th November 2012 and was done as a third party audit on behalf of MEG Group, Netherlands.

• GMP pharma consultants audited Glochem Industries, Unit-3, formulation unit as per international GMP norms on behalf of JSK Regulatory Services, UK on 21st November 2012.

• GMP Pharma consultants conducted a training programme at Hemmo Pharma, Mumbai on 19th November 2012 on the subjects of stability studies and investigation of OOS results to select Supervisors and Managers. The programme was well received.

• On 18th October 2012, GMP Pharma inspected the stuffing operations of the containerisation process at Fresenius Kabi, Pune. This was done on behalf of MEG Group, Netherlands.

• On 16th October 2012, GMP Pharma audited Maneesh Pharmaceuticals (on a third part basis), Mumbai for GMP compliance of injection products made on behalf of MEG Group, Netherlands.

• GMP Pharma audited Maneesh Pharma, Mumbai, for manufacture of parenterals, on behalf MEG group, Netherlands.

• GMP Pharma consultants conducted a full day programme on Pharma Industry – an awareness programme for managers of State Bank of Hyderabad on 3rd September 2012.

• GMP Pharma consultants audited Fresenius Kabi, Santiago, Chile, a sterile product manufacturing facility for GMP compliance on 27th and 28th August 2012. This was done on behalf of MEG export, Netherlands.

• GMP Pharma consultants have got an one year contract for upgrading quality systems of ZIM laboratories, Kalameshwar, Nagpur.

• GMP Pharma consultants has audited Fourrts Laboratories , Chennai as Third party auditors on behalf of MEG Group , Netherlands on 9th June 2012.

• GMP Pharma has started teaching Regulatory affairs and Intellectual property rights to students of M Pharm, Vishnu Institute of Pharmaceutical education and research, Narasapur, Medak District, Andhra Pradesh.

• GMP Pharma conducted a training on “General aspects of quality management” to officers and managers of Sangam Healthcare, , Medchal , Andhra Pradesh manufacturers of Diagnostic kits on 5th June 2012.

• MP Pharma have conducted an audit of Kontest chemicals P Limited on 4th June 2012 for compliance with GMP.

• GMP Pharma consultants have audited VIFOR India P Limited , a sterile manufacturing facility, manufacturing water for injection located at Kandla Economy zone at Gandhidam, Gujarat on 31st May 2012 on behalf of MEG group, Netherlands.

• GMP Pharma consultants have audited Marck Biosciences , a sterile manufacturing facility, located at Ahmedabad on 28th, 29th and 30th May 2012 , on behalf of MEG group, Netherlands.

• Dr Reddy's laboratories have given GMP Pharma consultants a contract with respect to regulatory compliance packaging materials.

• AA Capital India Development Fund LLC, with headquarters in London, asked GMP Pharma consultants to review and assess the processes of ZIM Laboratories, Nagpur and submit a report. They intend utilizing this report to take investment decisions. The project was completed on 9th and 10th May 2012.

• GMP Pharma consultants have been awarded a contract to bring the documentation of Camphor and Allied Products, Barielly, UP as per current GMP norms. This is a 9 month project.

• GMP Pharma consultants have vetted the drawings of API unit of Forrel Laboratories, for compliance with cGMP and have their opinion. The proposed facility will come up in Vishakapatnam.

• GMP Pharma have submitted concise project report for the proposed analytical laboratory to be set up by Pharmaexcil in Andhra Pradesh, Himachal Pradesh, Maharashtra and Gujarat.

• State bank of India, has given GMP Pharma consultants a project for assessing the techno economic viability of M/s VIVIN Laboratories Limited prior to their sanctioining the loan.

• GMP Pharma consultants have conducted a workshop for managers of SBI on an "overview of pharmaceutical industry" on 26th August 2011.

• GMP Pharma consultants are now conducting a techno economic viability study of M/s VIVIN laboratories Ltd. This assignment is through SBI.

• GMP Pharma consultants have got Techno Economic viability studies to be conducted of three companies namely, SMS Pharmaceuticals Limited – Vijayanagaram, Cheminova Remedies – Hyderabad, Mount Mettur Pharmaceuticals – Chennai (a Unit under revival).  All these are a part of the assignment given by State bank of India.

• Sri S R Parthasarathy addressed the conference "Pharma Contract Manufacturing 2011" at Mumbai on 10th October 2011 and spoke on "Recent trend in validation " and "Technology transfer". This was attended by 65 decision makers from leading Pharmaceutical industries. This was was organized by UBM Indian Pvt Limited.

• GMP Pharma consultants have audited M/s.Enal Drugs Pvt Limited, a Hyderabad based API manufacturing unit as per EU norms on 11th and 12th October 2011.

• GMP Pharma consultants conducted a third party audit of Dr Reddy’s laboratories CTO Unit-I on behalf of Laboratories CINFA, Spain.

• GMP Pharma Consultants audited M/s.Oman Pharmaceutical Products Company, Salalah on behalf of Cinfa, Spain in the first week of December, 2011.

• GMP Pharma consultants took part in a debate on “Challenges facing SME Pharma sector” organized by SBI and UTV Bloomberg on 11th February 2012 at Hyderabad. This will be telecast shortly . GMP Pharma consultants was represented by Dr S R Parthasarathy and C. Suresh babu.

• GMP Pharma consultants audited MRK Tubes, Silvassa, a collapsible tube manufacturer for quality compliance – as a third party auditor for Oman Pharmaceuticals, Salalah, Oman.

• GMP Pharma consultants conducted an audit of Analytical division of SIPRA Laboratories Limited on 9th March 2012 on behalf of Oman Pharmaceuticals LLC, Salalah.

• GMP Pharma consultants took audit of CIRON Drugs and Pharmaceuticals Pvt Limited, Boisar, Tarapur. This audit covered their sterile operations. This audit was conducted on a third party basis on behalf of Medical exports Group, Netherlands.

• GMP Pharma consultants took up audits of manufacturers of Neomycin Sulphate, Sodium Bicarbonate, Aspartame and Citric acid in China during the week 19th to 23rd March 2012. These were third party audits conducted on behalf of Oman Pharmaceuticals Company, Salalah.

• GMP Pharma Consultants audited the following companies in China for compliance with cGMP as a part of third party audit on behalf of Oman Pharmaceutical Products Company LLC, Salalah, Oman during March 19-23, 2012:
(a) JIALI BIO GROUP (QINGDAO) LIMITED, ShanDong, China
(b) CHANGZHOU GUANGHUI BIOTECHNOLOGY CO. LTD., Changzhou, Jiansu, China
(c) HUASHU PHARMACEUTICAL CORPORATION, Shijiazhuang, China
(d) HEBEI HUACHEN PHARMACEUTICAL CO. LTD., Hebei, China