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August 2017

QbD & PAT

August 28 - August 29
Citywest Hotel, Dublin Ireland, Saggart, Co.
Dublin, Ireland
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QbD & PAT conference will bring together participants from industry, academia and regulatory creating invaluable opportunity to discuss the recent developments, future trends, challenges and Solutions for development & Manufacturing of Pharmaceutical & Biotechnology products.The conference will focus on discussing the existing challenges and explore practical applications related to drug development, manufacturing and regulatory. Its a 2 day program which will include presentations, talks, case studies, panel & Round-table discussions from industry leaders, solution providers and academia

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Pharma CMI 2017

August 28 - August 29
HOLIDAY INN MUMBAI INTERNATIONAL AIRPORT, Sakinaka Junction, Andheri Kurla Road, Andheri East, Safed Pul, Sakinaka
Mumbai, Maharashtra 400072 India
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PHARMA CMI, is the only gathering of senior level professionals from Pharma, Biotech and Device professionals looking for the latest updates and learn about the most critical and relevant issues facing the competitive & Market Intelligence community. The conference theme is “Driving the future of Pharma Business through Competitive & Market Intelligence”. The conference aims to understand how the pharmaceutical & Biotech companies, marketing, competitive intelligence, strategic and operational divisions are staying updated with accurate information about their competitors in…

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September 2017

The Data Integrity 2017 | Hyderabad, India

September 18 - September 19
Radisson Blu Plaza Hotel, 8-2-409, Road Number 6, Banjara Hills, Green Valley, Banjara Hills
Hyderabad, Telangana 500034
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Data Integrity is a fundamental element of a (Bio) pharmaceutical industry to ensure quality and safety of drugs. It’s a major global concern of health authorities and (Bio) Pharma companies. Although Data Integrity is not a new issue, it has gain alarming attention in last few years due to FDA’s and MHRA’s scrutiny and a number product detention, import alerts, suspension of marketing authorization and warning letter issued to companies found non-compliant.  With the growing importance of the Indian pharmaceutical industry…

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Computer System Validation 2017 | Hyderabad, India

September 18 - September 19
Radisson Blu Plaza Hotel, 8-2-409, Road Number 6, Banjara Hills, Green Valley, Banjara Hills
Hyderabad, Telangana 500034
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The workshop is designed to provide attendees with the knowledge and working skills on complying with the requirements with GCC regulations Module 3 including Data Integrity, which is the current, focus regulatory audits worldwide. It addresses GCC Module 3 topics such as Pharmaceutical Quality Systems Elements (PQSE), Data Integrity elements, Corrective and Preventive Action (CAPA) and Computer Systems Validation (CSV).

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Pharma Quality Systems 2017 | Hyderabad, India

September 18 - September 19
Radisson Blu Plaza Hotel, 8-2-409, Road Number 6, Banjara Hills, Green Valley, Banjara Hills
Hyderabad, Telangana 500034
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A Pharmaceutical Quality Systems is mandatory to comply with EU GMP and the manufacturer shall establish and implement an effective pharmaceutical quality assurance system, involving the active participation of the management and personnel of the different departments.Learn all relevant aspects to implement and/ or improve Pharmaceutical Quality System fulfilling regulatory and GMP requirements. You will get to know the history of GMPs to product lifecycle management expectation of regulatory agencies. You will also have the possibility to learn on practical examples and…

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The Data Integrity 2017 | Mumbai, India

September 21 - September 22
HOLIDAY INN MUMBAI INTERNATIONAL AIRPORT, Sakinaka Junction, Andheri Kurla Road, Andheri East, Safed Pul, Sakinaka
Mumbai, Maharashtra 400072 India
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Data Integrity is a fundamental element of a (Bio) pharmaceutical industry to ensure quality and safety of drugs. It’s a major global concern of health authorities and (Bio) Pharma companies. Although Data Integrity is not a new issue, it has gain alarming attention in last few years due to FDA’s and MHRA’s scrutiny and a number product detention, import alerts, suspension of marketing authorization and warning letter issued to companies found non-compliant.  With the growing importance of the Indian pharmaceutical industry…

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Computer System Validation 2017 | Mumbai, India

September 21 - September 22
HOLIDAY INN MUMBAI INTERNATIONAL AIRPORT, Sakinaka Junction, Andheri Kurla Road, Andheri East, Safed Pul, Sakinaka
Mumbai, Maharashtra 400072 India
+ Google Map

The workshop is designed to provide attendees with the knowledge and working skills on complying with the requirements with GCC regulations Module 3 including Data Integrity, which is the current, focus regulatory audits worldwide. It addresses GCC Module 3 topics such as Pharmaceutical Quality Systems Elements (PQSE), Data Integrity elements, Corrective and Preventive Action (CAPA) and Computer Systems Validation (CSV).

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Pharma Quality Systems 2017 | Mumbai, India

September 21 - September 22
HOLIDAY INN MUMBAI INTERNATIONAL AIRPORT, Sakinaka Junction, Andheri Kurla Road, Andheri East, Safed Pul, Sakinaka
Mumbai, Maharashtra 400072 India
+ Google Map

A Pharmaceutical Quality Systems is mandatory to comply with EU GMP and the manufacturer shall establish and implement an effective pharmaceutical quality assurance system, involving the active participation of the management and personnel of the different departments.Learn all relevant aspects to implement and/ or improve Pharmaceutical Quality System fulfilling regulatory and GMP requirements. You will get to know the history of GMPs to product lifecycle management expectation of regulatory agencies. You will also have the possibility to learn on practical examples and…

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October 2017

Para Injecto 2017

October 19 - October 20
HOLIDAY INN MUMBAI INTERNATIONAL AIRPORT, Sakinaka Junction, Andheri Kurla Road, Andheri East, Safed Pul, Sakinaka
Mumbai, Maharashtra 400072 India
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“Para-Injecto 2017 - The world of Parenterals and Injectables” conference and training, will be unveiling the challenges and exploring solutions in Formulation & Development, Manufacturing, packaging, Quality and Regulatory aspects of Parenterals and Injectables. The Para-injecto conference is a perfect platform to showcase and discuss with the industry leaders the recent advances, latest technology and alternative strategies that are flexible and cost-effective to develop and manufacture Parenterals & Injectables. Renowed Industry Leaders, Regulatory Experts, Academia, Solutions providers and Manufacturers from…

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