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Conferences on July 19, 2012

Academy of World Business, Marketing and Management Development

Date: 16-Jul-12 to 19-Jul-12
Location: Budapest / Hungary
Manuscripts for this conference are invited in any of the various track areas listed on our website which include marketing, management, finance, banking, accounting, tourism, psychology, sociology, information technology, economics, etc The deadline for abstracts/proposals is 4 November 2011.

Bioplasma World Asia 2012

Date: 18-Jul-12 to 19-Jul-12
Location: Hong Kong / China
Bioplasma World Asia 2012 is Asia-Pacific’s ONLY conference focusing on plasma and plasma-derived products. To be held in Hong Kong on July 18-19th,it will bring together Asian and international plasma fractionators, blood establishments, health authorities, regulators, and technology specialists to discuss pressing issues, share best practices, and explore opportunities and viable partnerships to further drive the Asian bioplasma industry forward and achieve the much sought-after self-sufficiency. Bioplasma World Asia will feature case studies and spirited discussions led by a world-class line up of thought leaders and practitioners who will influence the growth of the bioplasma industry. Market trends, regulatory challenges, quality issues, best practices in plasma collection and ...

HR Policies for Small Companies/Organizations

Date: 19-Jul-12 to 19-Jul-12
This 90-minute webinar provide you a comprehensive understanding of HR policies that small companies need to have, information on the number of employees you can have before you must have these policies in place, and save you from penalties and fines.

Live webinar on Medical Device Adverse Event Reporting in EU, Canada and US by compliance2go

Date: 19-Jul-12 to 19-Jul-12
Location: Houston / Texas / United States
This webinar is intended to help you get familiar with the medical device adverse event reporting requirements during clinical studies and post-marketing in the EU, Canada and US

Cleanroom Management – From a Microbial Perspective

Date: 19-Jul-12 to 19-Jul-12
This 90-minute webinar will present a scientific, risk-based approach to cleanroom management to help you ensure production of contamination free products that are safe for human use.

Designing an Effective Cleaning Validation for Reusable Medical Devices in Today's Regulatory Environment

Date: 19-Jul-12 to 19-Jul-12
This webinar will address the most current (regulatory) expectations for cleaning validation of reusable medical devices that are performed in support of the instructions in the instruction for use (IFU).

How to Prepare for a Tag Along Audit of CFR 21 Part 11 - Webinar By GlobalCompliancePanel

Date: 19-Jul-12 to 19-Jul-12
Location: Aba / Delaware / United States
Overview: Regulatory compliance requirements for CFR 21 Part 11/Annex 11 (also known as ERES) have undergone several revisions since its inception during the late 1990s. While the agencies have endeared themselves to the industry by adopting a flexible audit approach for ERES, they are increasingly requiring companies to comply with the regulations. Increased number of citations and the recently announced "tag along" audit approach is a gentle reminder of things to come by way of stricter enforcement of Part 11/Annex 11. It is critical that the industry becomes familiar with the intricacies of the regulation so as to ensure that audits of their systems in this area are citation free. Why should you attend: It has been close to a decade since the US FDA published their ...

IEC 62304 for Medical Device Software Development: Steps to Compliance - Webinar By GlobalCompliancePanel

Date: 19-Jul-12 to 19-Jul-12
Overview: IEC62304 is a internationally recognized software lifecycle standard. The risk dependent activities and documentation requirements necessary for compliance with this document will be explained. Questions like: How much detail is required in the requirement specification? What is a software unit? How can integration testing be performed without test harnesses? will be answered. Practical guidance on how to employ a streamlined but yet compliant development process will be given. Why should you attend: This webinar will explain basic design control concepts and the criticality dependent requirements for software development. Software specification, architectures and resulting design documentation will be discussed, as well as practical tips on how to streamline the ...

The FDA Inspection Process: From SOP to 483 - Webinar By GlobalCompliancePanel

Date: 19-Jul-12 to 19-Jul-12
Overview: Does the FDA call in advance or just show up at my door? Where do I let the inspector go? Do I give them a tour? What should I let them see? Who should I let them talk to? Are they ever going to leave? The FDA inspection is the most nerve-wracking event in the life of a regulatory professional - you're in charge of compliance, usually in the background, and NOW you're in the spotlight, and if your performance isn't good, it's not the show that may close, it's YOUR COMPANY! However, adequate planning, training, composure, and understanding should result in many encore presentations! This session will discuss how to prepare for the inspection, what to do during the inspection and the close-out interview, and how to respond to the inspection. Also contained in this session will ...

ISACA Issues Guidance on Securing Sensitive Personal Information: Using COBIT 5 For India’s IT Act

Date: 18-Jul-12 to 19-Jul-12
Location: India
Webinar on guidance on the best approach to secure sensitive personal data or information using the COBIT 5 framework on 18th July 2012 ISACA's virtual conference which will help enterprises ensure safe, productive business use of mobile devices and understand mobile application ecosystems, mobile security threats and corresponding business risks titled Mobile Security Imperatives 2012. The conference also will address privacy and security challenges of Bring Your Own Device (BYOD) under the EU privacy and data protection legislation on 19th July 2012