Events tagged "Control":

3rd International Conference on Smart Materials and Nanotechnology in Engineering

December 5, 2011toDecember 8, 2011

Shenzhen, China

The field of Smart Materials and Nanotechnology is very diverse with application ranging from bioengineering to photonics. However, the emphasis for this conference will be on their applications in aerospace. This does not preclude novel developments in smart materials and nanotechnology for other areas as a means of greater understanding of the basic properties and capabilities of this new class of materials. Read more »

PMP Exam Prep Training in Jeddah Saudi Arabia

Ramada Continental Hotel
Jeddah, Saudi Arabia

PMP Exam Prep Training in Jeddah Saudi Arabia logoBusiness Solutions Est. offers training of this highly demanding and top paid certification in the world.

BSE is approved Global REP(Registered Education Provider) by PMI®.

Put your career on the fast track with the PMP certification, which is aimed at experienced business professionals looking to bolster their resume with this lofty designation. Read more »

Change Control Under the cGMPs and How the Regulations are Changing

Online Event

Change Control Under the cGMPs and How the Regulations are Changing logoWhy Should You Attend:

This webinar will provide valuable information on the requirements of an effective change control process from an operational and regulatory perspective. It will describe how and when to implement a system that is both cost effective and compliant, in an ever-changing regulatory landscape, keeping appropriate control over the processes and products without burdening the business. Read more »

International Siberian Conference On Control And Communications

Krasnoyarsk Business Center, Krasnoyarsk, Russia

The 9th Siberian conference SIBCON-2011 aims to offer opportunities to learn and to share information on the latest advances in communications and control systems. It will be held in Krasnoyarsk, the Russian Federation, on September 15-16, 2011. The conference is organized by the IEEE on a regular basis in order to promote interdisciplinary discussion and interaction among scientists and engineers with an emphasis on the IEEE membership. Read more »

Understanding ISO 13485 vs. ISO 9001 for Successful QMS in Medical Device Industries – Webinar By GlobalCompliancePanel

Online Training Webinar

ISO 13485:2003 is a quality management system standard specially written for the medical device industry and is on the U S Food & Drug Administration (FDA) list of recognized consensus standards. Read more »

Chemical Control for Food Manufacturers: Ingredient, Cleaning and Hazardous Materials – Webinar By GlobalCompliancePanel

Online Training Webinar

Overview: A comprehensive review of an ideal chemical control program will be presented.

The guidelines presented will enable your company to implement programs that are cost effective and meet or exceed the expectations of major QSR, and GFSI audit criteria. Read more »

Maquiladoras/IMMEX Compliance – Webinar By ComplianceOnline

Online Event

Maquiladoras/IMMEX Compliance   Webinar By ComplianceOnline logoWhy Should You Attend:
If you have an IMMEX plant, are planning to incorporate one, or do business or deal with an IMMEX, this webinar is for you. It will help you understand how these plants are controlled and operated, and why specific documentation and information is required by various parties in the supply chain. Read more »

COSO ERM Simplified – Webinar By ComplianceOnline

Online Event

COSO ERM Simplified   Webinar By ComplianceOnline logoWhy Should You Attend:
Enterprise Risk Management or ERM’s primary purpose is to improve the quality of decision-making throughout an organization. Implementing ERM may seem like a daunting task but when one gets a grasp on what it is, and then it becomes easier to understand how it can be implemented. Read more »

Webinar: Submission Documentation for Sterilization Process Validation

Online Event

Webinar: Submission Documentation for Sterilization Process Validation logoWhy Should You Attend:
Having a plan for gathering and compiling appropriate sterility assurance documentation to be included in a global marketing application is essential for injectable drug products. In this session we will provide an overview of current regulatory guidance and compendial requirements associated with sterilization validation and control of microbial quality. Read more »

A Comparison of ICH Q-10 Quality System and the FDA Quality Systems Approach

Online Event

A Comparison of ICH Q 10 Quality System and the FDA Quality Systems Approach logoWhy Should You Attend:
The QSA to Pharmaceutical cGMPs and ICH-Q10 are guidance documents that stress the importance of management’s responsibilities to meet customer needs by encompassing quality improvement through quality by design QbD), risk management, process control, and user feedback and experience. Read more »

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