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MAY 14 - 15, 2020

HYDERABAD, INDIA

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ManuPharmaNext Conference 2020 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.

CONFERENCE HIGHLIGHTS

  • Big Data and Blockchain
  • Process Improvement
  • Aseptic Technology & Cleaning Validation
  • Pharma 4.0 – Automation, AI, IoT
  • Transitioning to Continuous Manufacturing
  • MES
  • cGMP & FDA Guidelines
  • Data Integrity

This two-day 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
  • 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

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