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donderdag 11 januari 2018

HSE eBulletin service Daily Digest Bulletin

HSE e-Bulletin service
Pressure systems awareness course - 25 January

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This course will offer delegates the unique opportunity to learn from real life case studies and forensic investigations into pressure systems failures, providing a first hand perspective of what can go wrong and why. 

On completion of this course delegates will be able to identify pressure systems in the workplace and and understand which legal requirements apply to this equipment. 

Delegates will develop a firm understanding of the nature and significance of common risks associated with pressure systems, who has duties under the regulations and current risk mitigation strategies.



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Practical Management of LEV controls course - 30 January

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Practical Management of LEV controls

Tuesday 30 January 2017
Training & Conference Unit, Harpur Hill, Buxton, SK17 9JN

We are running a BOHS approved course on Practical Management of Local Exhaust Ventilation Controls. 

Book your place here

training

The course will demonstrate how to successfully manage LEV controls in order to get effective, efficient, and reliable control of airborne contaminants, at least cost. 

This innovative, practical and lively course was developed - and will be delivered - by Dr Mark Piney (former HSE Principal Specialist Inspector, main author of HSE LEV guidance), along with other HSL specialists in LEV. 

This course is British Occupational Hygiene Society (BOHS) endorsed.

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Pesticides e-bulletin: CRD Event - Two Day Efficacy Workshop: The presentation and interpretation of Efficacy trials data in Biological Assessment Dossiers to support authorisations under EC 1107/2009

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Welcome to the HSE Pesticides eBulletin

This e-bulletin is from HSE's pesticides team

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Two Day Efficacy Workshop: The presentation and interpretation of Efficacy trials data in Biological Assessment Dossiers to support authorisations under EC 1107/2009

HSE's Chemicals Regulation Division (CRD) is running a two day workshop which will provide an overview of the importance of efficacy trial design and trials reports, how to approach and critically assess data, and effective presentation of data in a Biological Assessment Dossier (BAD). The outcomes are also to develop an understanding of how the data support the proposed GAP and National labels for product authorisations. This largely practical workshop will use data examples to help attendees improve their BAD writing by understanding the regulatory approach, common problems, and identifying best practice. Time will be available during the workshop for some group discussion of specific applicant questions relating to their own data.      

The workshop will be held at the Chemicals Regulation Division in York on Tuesday 27th and Wednesday 28th March, 2018.  Registration will begin from 9:15 am.  The workshop will start at 9:45 am on day one and finish around 4:00 pm on day two.  The cost per delegate to attend the workshop will be £650 (plus VAT).

 

Topics of discussion

  • Worked examples and practical sessions (approximately 80% of time)
  • The importance of effective trials design and trial reports
  • Collation and critical assessment of trials data
  • Principles of data presentation in the BAD
  • Examples of effective and flawed approaches
  • Common errors and problems
  • Use of the BAD to devise and support dRRs, GAPs and National product labels
  • Group discussion of applicant questions (details of question scope and how to submit questions will be provided after course sign-up)  

Target Audience

This course is suitable for those involved in designing and conducting efficacy trials, assessing trials data, and writing efficacy BADs and draft registration reports for submission to regulatory authorities. No prior experience in this area is assumed, and the course is suitable for beginners as well as more experienced BAD writers.  The primary focus of this workshop is the use of practical realistic examples to help attendees understand how regulators review the BAD and associated dRR, and how to effectively meet regulatory requirements. However, attendees should be familiar with 1107/2009 efficacy data requirements, associated EPPO standards, and the regulatory framework, as these will not be covered in detail in this workshop.  This course may be of interest to previous attendees of the companion efficacy workshop 'Requirements and Assessment under EC 1107/2009'.

 

Registrations

Because of the nature of the event, places will be limited to a maximum of 16 people, and will be issued on a first-come first-served basis.

If you wish to register for the above workshop please visit http://www.hsl.gov.uk/crd and complete an online registration form. The closing date for applications is the 28th February 2018.

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