Pharmaceutical Manufacturing Conference

DECEMBER 3 - 5, 2020

VIRTUAL CONFERENCE

DOWNLOAD BROCHURE

As we continue to monitor the global impact of COVID-19, and as the world evolves, so do we.
We are transforming this event to be fully digital: The ManuPharmaNext Conference 2020 - Virtual

Pharmaceutical Manufacturing; ManuPharmaNext Conference – 2020 (The First Ever Comprehensive Pharma Manufacturing Virtual Conference) will explore business, regulatory, and technical aspects associated with adopting novel manufacturing platforms to production of pharmaceuticals. Learn more on how innovations and regulations are working in tandem toward the modernization of the pharmaceutical industry.

 

Focus areas will include the integration of Pharma 4.0, Digital Manufacturing Intelligence, Manufacturing Execution System, Industrial Internet of Things, regulations, and compliance on drug manufacturing as well as recent developments in the pharmaceutical and biopharmaceutical industry, among others. Presentations and discussion will revolve around critical approaches for successful manufacturing and leveraging quality as a competitive advantage.

 

The event is interactive and encourages the active participation of all attendees. Methodologies used in the lectures are workshops, keynotes and discussion sessions. We encourage delegates to use this opportunity to bring questions from your own practice up for discussions.

With ongoing digital transformation to ensures business continuity at all times, we bring you Global Experts at your fingertips. You’ll have opportunities to network with your fellow attendees and presenters, just like you would at our in-person events. Engage throughout the sessions, via the live chat, and during dedicated networking breaks and events.

 

During the conference, you can view presentations, access PDFs of the presentations, take downloadable notes in each session, participate in polls, chat with other attendees, and participate in LIVE Q&A sessions and Group Discussions with speakers.

 

At Compliance Trainings’ Virtual Conference, save time and ensure enhanced knowledge at ease.

Featured Speakers from our Previous Conference

Our speakers come from all over the globe. You’ll hear from renowned industry leaders and visionary designers.

Chinmoy Roy

Data Integrity, CSV and Process Automation SME

Internationally recognized SME in the areas of CSV, GAMP, Data Integrity, CFR 21 Part 11, Annex 11 and Quality Risk Management.

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Orlando Lopez

E-Compliance and E-Records Quality SME

Renowned author and e-compliance and e-records integrity regulations and guidelines expert (21 CFR Part 11, Annex 11, MHRA, WHO, PIC/S, CFDA, USFDA, EU OMLC).

David Nettleton

CSV and FDA Compliance Specialist

Renowned CSV Author and FDA Compliance Specialist for 21 CFR Part 11, HIPAA, and Computer System Validation.

Nichola Stevens

Current Chair of GAMP UK

Principal Computer System Validation & IT Quality Consultant and CEO of Nuncius Compliance Solutions Ltd. and current Chairperson of the GAMP UK Steering Committee

Computer System Validation

Carolyn Troiano

CSV & FDA Expert

30+ years of experience in CSV & large-scale IT system implementation projects. Collaborated with FDA and other industry representatives on 21 CFR Part 11 back in the mid-1980s,.

Trev Simmons

Consultant, TS CSV QA Ltd., UK

CSV and IT auditor for both internal and external computerized systems / suppliers across GLP, GMP and GCP.

Galit Lisaey

Gal.IT Data Integrity Consulting, ISRAEL

Thomas HALFMANN

Global Head Production IT, NNIT, Switzerland

Jens Seest

Service Delivery at Pharma IT, Germany

Timur Kabadayı

MD at CONVALgroup, Turkey

Computer System Validation

KalpeshKumar Vaghela

CEO of Infra Control Systems

30+ years’ experience as Software Validation Specialist, GAMP5 and 21 CFR Part 11 Compliance

Heloisa Cytrynbaum

QMS & Data Integrity Expert, Brazil

QMS and DI Expert and Inspections with FDA, MHRA, ANVISA and INVIMA

Previous Keynote Speakers

Learn and Network with the best in the Industry. The ultimate Pharma Manufacturing experience!

Ranjit Barshikar

QbD / cGMP Consultant

Mayur Parmar

ex-Drugs Inspector, FDA Gujarat

Sachin Bhandari

GM, Head CSV

SUN PHARMA Ltd

Suryamohan Surampudi

Head – Electronic Data Systems Compliance, Plant IT Systems & Automation

Dr Reddy’s Laboratories

Ms. Rana Golzar

CSV Expert

Iran

Aniruddha Mehta

Head QA-IT

Alembic Pharma

Computer System Validation

Anand Rao. C

Associate Vice President,
Head QA and CSV

Navitas Life Sciences

Venkat Srinivas

GM–Information Services, APAC Hub Lead

Apotex India

Mrs. Balwinder Kaur

Pharmaceutical Expert Trainer

Hari Vayas Bansal

Director & GxP Compliance Consultant

GxP Pharma Traine

Computer System Validation

Sudhir Kumar Gupta

Lead Quality , IT Department – Biopharma Division

Intas Pharmaceutical

Damodharan Muniyandi

Global Quality and Regulatory Affairs

SAI LIFE SCIENCE

Key Areas Covered

  • Future of Pharmaceutical QMS
  • cGMP & FDA Guidelines
  • GMP Inspections
  • Quality Metrics
  • Process Validation
  • API manufacturing
  • Formulation Development
  • Data Integrity
  • Pharma 4.0 – Automation, AI, IoT
  • Continuous Manufacturing
  • Analytical Procedures
  • MES
  • Big Data and Blockchain
  • Cyber Security

This year’s ManuPharmaNext Conference is geared for Pharmaceutical and biopharmaceutical companies functioning in the areas of manufacturing, operations and regulations. You will have the opportunity to take-home cutting-edge developments methodologies and strategies. Also, get answers and updates to the below:

  • Why the industry needs to embrace new ways to develop and manufacture medicines
  • How manufacturing needs to adapt to new modalities
  • The impact of the wave of disruptive technologies referred to as Industry 4.0, including Industrial Internet of Things (IIoT), machine learning (ML), automation, robotics, advanced analytics, etc.
  • The role of continuous manufacturing in modernizing pharmaceutical industry
  • How the industry can learn from innovations in other industries
  • The benefits of advanced process control.. and many more.

Recent EU and FDA inspection documents prove that qualification, validation and electronic laboratory records are on target of inspectors. The time has never been more critical to evaluate and ensure your organization has top-notch compliant procedures. To ensure that companies successfully pass Regulatory inspections and to also make sure that companies smoothly adopt latest tools & technologies available for validation, Compliance Trainings is pleased to announce the “CSV & IT Systems Validation Virtual Conference – 2020”.

  • Connect with Manufacturing, Production, Quality and Operations experts within the Pharmaceutical industry with decades of experience
  • The conference will focus on both API as well as Formulation development
  • Stay Up-to-Speed with Pharma 4.0
  • Shape and magnify your understanding of the regulatory requirements and expectations in pharmaceutical manufacturing
  • Excellent networking opportunities to build relationships
  • Branding opportunities as well as taking advantage to meet potential clients face-to-face.

Industries
  • Pharmaceuticals
  • Medical Devices
  • Manufactures of APIs
  • Finished Products
  • Quality Control Laboratories
  • Contract Laboratories
  • Clinical Research Organizations
  • Biotechnology
  • Pharma Chemicals
  • Radiological Health
  • Regulated Food
  • Cosmetics
  • Pharma Software Developers
  • Automation & IT Companies

Departments
  • QA & QC
  • Regulatory Affairs
  • Research and Development
  • Training Departments
  • IT Departments
  • Documentation
  • Engineering
  • Manufacturing
  • Validation
  • Production
  • Laboratory Departments
  • Operations
  • Software Development
  • Facilities

Professionals
  • Directors, VP’s, CxO’s
  • General Managers
  • Senior Managers & Managers
  • Supervisors & Team Leaders
  • Validation Specialists
  • Documentation Specialists
  • Research Scientist
  • Project Managers
  • Analytical Chemists
  • Training Specialists
  • Auditors
  • Clinical Data Specialists
  • Technicians
  • Vendors & Suppliers

Testimonial

WHAT OUR PAST DELEGATES HAD TO SAY
Very well organized. Seminar was interactive and informative. Such an event must be conducted more often

HOD

Quality

By far, this has been on of the best seminar we have attended. Highly recommended.

General Manager

IT/QA

This is the third time our team has attended a Compliance Trainings seminar, and they never fail to provide better experience each time

Director

Quality

Perfect workshop to understand how to avoid warning letters and 483's. Highly recommended seminar. Please let us know when the next session will be held.

Sr. Director

Quality

Perfect workshop to understand how to avoid warning letters and 483s. Highly recommended seminar. Please let us know when the next session will be held. I would like more from our team to attend.

Sr. Director

Quality

Such a training is always required for directions to implementing guidelines. Brilliant session. Great interactive session with some of top-notch experts from the industry.

Asst. Vice President

Quality Assurance

The seminar was extremely helpful and informative along with current scenario examples. Our team had a great learning experience.

General Manager

Quality

Fill in the form to Download Brochure and Book your seats







With ongoing digital transformation to ensures business continuity at all times, we bring you Global Experts at your fingertips. You’ll have opportunities to network with your fellow attendees and presenters, just like you would at our in-person events. Engage throughout the sessions, via the live chat, and during dedicated networking breaks and events.

 

During the conference, you can view presentations, access PDFs of the presentations, take downloadable notes in each session, participate in polls, chat with other attendees, and participate in LIVE Q&A sessions and Group Discussions with speakers.

 

At Compliance Trainings’ Virtual Conference, save time and ensure enhanced knowledge at ease.

 

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