COMMUNICATION ALCHEMY

Date/Time
Date(s) - 07/03/2016 - 08/03/2016
12:00 am

Price: £1,100.00 (ALL UK EVENTS ARE SUBJECT TO VAT)

Conference Ref: R3-4216

Brochure Download:
3-4316_Communication Alchemy_W

Location
The Rembrandt Hotel

COMMUNICATION ALCHEMY

The Art of Winning People and Business Through Effective Communication Techniques

WHY YOU SHOULD ATTEND

We live in a world surrounded by an ocean of global
communication and more choice than ever before
as to how we interact with others – you need to ensure
you are heard above all of this frenzied communication
traffic and communicate to win.

This two day course will challenge your current
thinking and behaviour in all areas of
communication. Through a host of practical exercises,
tools and techniques you will explore the impact of
your communication style in winning over people,
situations and business. The tools and techniques
you will learn will positively change the way you
communicate in every situation with power, passion
and enhanced purpose.

KEY TOPICS TO BE COVERED:

  • Understand the benefits of using Enhanced Thinking and Dynamic Action
  • Invisible PowerPoint – Creating Communication that works
  • How to be heard, listened to and have real impact in the office
  • Gain an insight into body language and the art of mind reading

COURSE LEADER

Nick Looby, Feet on the Ground Training

If you have any queries please click here to contact Sarah Spanswick

 

Event Booking Form

*Asterisks are required fields

Price

£1,100.00

£220.00

£1,320.00

Booking Information

Are you the delegate?
Is this a Group Booking?
Are you booking on behalf of someone else?

I confirm I have read and understood the Terms and Conditions

Booker's Details

Company Details

Invoice Company Details

Areas of Interest

Agrochem
Animal Health
GMP
IP
Legal
Medical Devices
Pharmaceutical
Biotech
Management Skills
Support Staff Development

Marketing Details

Brochure mailed to you
Brochure passed to you
Journal/Magazine Ad
Journal/Magazine Insert
Our Website
Web Search
Returning Customer
Recommendation
Other

Send your Booking


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ADVANCED PHARMACOVIGILANCE

Date/Time
Date(s) - 14/03/2016 - 16/03/2016
All Day

Price: £1,700.00 (ALL UK EVENTS ARE SUBJECT TO VAT)

Conference Ref: A3-4016

Brochure Download:
3-4016_Advanced Pharma_W

Location
The Rembrandt Hotel

ADVANCED PHARMACOVIGILANCE

This Advanced Pharmacovigilance course is designed for those with at least 2 years worth of knowledge in Drug Safety and will provide a comprehensive, yet practical assessment of the main Regulations required to produce a compliant reporting Company:-

BENEFITS OF ATTENDING

  • Expand your Global Safety Knowledge
  • Enhance your Team’s capabilities and compliance in both the Regulations and your Company’s expectations
  • Help ensure you build and maintain a quality Pharmacovigilance Department ready for any Pharmacovigilance Inspection
  • Participate in group workshop sessions and discuss how to apply the legislation to ensure compliance, especially to satisfy Regulatory Inspections

MEETING TIMES
14 March 2016

Registration & Coffee  09.00

Start: 09.30  – Finish: 1700

Drinks Reception:  17.00 –  18.00

15 March 2016  2015

Start: 09.00 –  Finish 17.00

16 March 2016

Start:  09.00  –  Finish:  16.30

 If you have a query please click here to contact Sarah Spanswick

Event Booking Form

*Asterisks are required fields

Price

£1,700.00

£340.00

£2,040.00

Booking Information

Are you the delegate?
Is this a Group Booking?
Are you booking on behalf of someone else?

I confirm I have read and understood the Terms and Conditions

Booker's Details

Company Details

Invoice Company Details

Areas of Interest

Agrochem
Animal Health
GMP
IP
Legal
Medical Devices
Pharmaceutical
Biotech
Management Skills
Support Staff Development

Marketing Details

Brochure mailed to you
Brochure passed to you
Journal/Magazine Ad
Journal/Magazine Insert
Our Website
Web Search
Returning Customer
Recommendation
Other

Send your Booking


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REGULATORY AFFAIRS FOR SUPPORT STAFF

Date/Time
Date(s) - 03/03/2016 - 04/03/2016
All Day

Price: £1,175.00 (ALL UK EVENTS ARE SUBJECT TO VAT)

Conference Ref:

Brochure Download:
3_4116_REGULATORY AFFAIRS FOR SUPPORT STAFF_W

Location
The Rembrandt Hotel

REGULATORY AFFAIRS FOR SUPPORT STAFF

The two-day Regulatory Affairs for Support Staff course provides an introduction to Regulatory Affairs and the basics of drug development and has been designed specifically for those working in a support staff role. The course will provide a thorough grounding in the subject of Regulatory Affairs and will enable you to perform in your role more effectively.

KEY TOPICS TO BE COVERED INCLUDE:-

• Learn about the Drug Development Process – from Drug  Discovery to Product Launch and Beyond
• Understand the Background of European Law – Regulations, Directives etc.
• Discover where you can find Information on Regulatory Affairs, Approvals, Withdrawals etc.
• How to Seek Scientific Advice in Europe
• What is the Common Technical Document
• The EMA; role and responsibilities
• Applying for a Marketing Authorisation in the EU
• What is the Centralised Procedure
• Decentralised, Mutual Recognition and National procedures
• Key Aspects of Drug Safety Reporting
• Pharmacovigilance and GCP Inspections
• Managing Product Labelling
• Discussion on Renewals and Variations
• Understand Parallel Trade and Generic Applications

SPEAKER

Norah Lightowler, Lightowler Associates

If you have any queries please click here to contact Sarah Spanswick

 

Event Booking Form

*Asterisks are required fields

Price

£1,175.00

£235.00

£1,410.00

Booking Information

Are you the delegate?
Is this a Group Booking?
Are you booking on behalf of someone else?

I confirm I have read and understood the Terms and Conditions

Booker's Details

Company Details

Invoice Company Details

Areas of Interest

Agrochem
Animal Health
GMP
IP
Legal
Medical Devices
Pharmaceutical
Biotech
Management Skills
Support Staff Development

Marketing Details

Brochure mailed to you
Brochure passed to you
Journal/Magazine Ad
Journal/Magazine Insert
Our Website
Web Search
Returning Customer
Recommendation
Other

Send your Booking


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PHARMACEUTICAL REGULATORY AFFAIRS IN AFRICA INCLUDING SOUTH AFRICA

Date/Time
Date(s) - To Be Confirmed

Price: £0.00 (ALL UK EVENTS ARE SUBJECT TO VAT)

Conference Ref: A10-4015

Brochure Download:

PHARMACEUTICAL REGULATORY AFFAIRS IN AFRICA ~ INCLUDING SOUTH AFRICA

South Africa, Nigeria, Ghana, Uganda, Tanzania, Algeria,
Morocco, Tunisia, French Speaking Africa

TOPICS TO BE COVERED AT THIS PHARMACEUTICAL REGULATORY AFFAIRS IN AFRICA MEETING:

  • Overview of The Regulatory Requirements
    within African countries
  • Company and Product Registration
  • Practical information on Compiling Dossiers
  • How to Comply with Regulatory Submission
    Strategy
  • Recent Developments in South Africa
  • Harmonisation and Co-operation Initiatives
    in Africa

FULL MEETING INFORMATION WILL BE POSTED SHORTLY IN THE MEANTIME IF YOU HAVE ANY QUERIES PLEASE CLICK HERE TO CONTACT SARAH SPANSWICK

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ESSENTIAL OVERVIEW OF THE PHARMA INDUSTRY

Date/Time
Date(s) - 25/09/2015
All Day

Price: £575.00 (ALL UK EVENTS ARE SUBJECT TO VAT)

Conference Ref: A9-4215

Brochure Download:
9-4215_ESSENTIAL OVERVIEW OF THE PHARMACEUTICAL INDUSTRY_W

Location
The Rembrandt Hotel

ESSENTIAL OVERVIEW OF THE PHARMA INDUSTRY

An Overview of Drug Development from Lab to Patient

If you have any queries please click here to contact Sarah Spanswick

BENEFITS OF ATTENDING THIS SEMINAR:

  • Increase your Understanding of the Pharma Industry
  • Develop your Knowledge of the Multiple and Complex
  • Stages of Drug Development from Drug Discovery through to Marketing
  • Understand the Roles and Responsibilities of Key
    Departments and how they Work Together
  • Get to Grips with the Phases of Clinical Trials and
    Regulatory Processes
  • How to Relate your own responsibilities and Understand
    the role of Others in the Process
  • Appreciate the Current Trends and Future Prospects
    for Global Drug Development

SPEAKER

Dr. Laura Brown, Course Director, School of Pharmacy, University of Cardiff and Independent Pharmaceutical Training Consultant

THIS COURSE CAN ALSO BE RUN IN-HOUSE, FOR MORE INFORMATION PLEASE CLICK HERE

Event Booking Form

*Asterisks are required fields

Price

£575.00

£115.00

£690.00

Booking Information

Are you the delegate?
Is this a Group Booking?
Are you booking on behalf of someone else?

I confirm I have read and understood the Terms and Conditions

Booker's Details

Company Details

Invoice Company Details

Areas of Interest

Agrochem
Animal Health
GMP
IP
Legal
Medical Devices
Pharmaceutical
Biotech
Management Skills
Support Staff Development

Marketing Details

Brochure mailed to you
Brochure passed to you
Journal/Magazine Ad
Journal/Magazine Insert
Our Website
Web Search
Returning Customer
Recommendation
Other

Send your Booking


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REGULATORY AFFAIRS FOR SUPPORT STAFF

Date/Time
Date(s) - 24/09/2015 - 25/09/2015
All Day

Price: £1,175.00 (ALL UK EVENTS ARE SUBJECT TO VAT)

Conference Ref: P9-4115

Brochure Download:
9-4115_REGULATORY AFFAIRS FOR SUPPORT STAFF_W

Location
The Rembrandt Hotel

REGULATORY AFFAIRS FOR SUPPORT STAFF

The two-day Regulatory Affairs for Support Staff course provides an introduction to Regulatory Affairs and the basics of drug development and has been designed specifically for those working in a support staff role. The course will provide a thorough grounding in the subject of Regulatory Affairs and will enable you to perform in your role more effectively.

PLEASE NOTE THAT WE WILL BE RUNNING THE REGULATORY AFFAIRS FOR SUPPORT STAFF MEETING AGAIN ON 3 & 4 MARCH 2016

KEY TOPICS TO BE COVERED INCLUDE:-

• Learn about the Drug Development Process – from Drug  Discovery to Product Launch and Beyond
• Understand the Background of European Law – Regulations, Directives etc.
• Discover where you can find Information on Regulatory Affairs, Approvals, Withdrawals etc.
• How to Seek Scientific Advice in Europe
• What is the Common Technical Document
• The EMA; role and responsibilities
• Applying for a Marketing Authorisation in the EU
• What is the Centralised Procedure
• Decentralised, Mutual Recognition and National procedures
• Key Aspects of Drug Safety Reporting
• Pharmacovigilance and GCP Inspections
• Managing Product Labelling
• Discussion on Renewals and Variations
• Understand Parallel Trade and Generic Applications

SPEAKER

Norah Lightowler, Lightowler Associates

If you have any queries please click here to contact Sarah Spanswick

 

Event Booking Form

*Asterisks are required fields

Price

£1,175.00

£235.00

£1,410.00

Booking Information

Are you the delegate?
Is this a Group Booking?
Are you booking on behalf of someone else?

I confirm I have read and understood the Terms and Conditions

Booker's Details

Company Details

Invoice Company Details

Areas of Interest

Agrochem
Animal Health
GMP
IP
Legal
Medical Devices
Pharmaceutical
Biotech
Management Skills
Support Staff Development

Marketing Details

Brochure mailed to you
Brochure passed to you
Journal/Magazine Ad
Journal/Magazine Insert
Our Website
Web Search
Returning Customer
Recommendation
Other

Send your Booking


Directions to The Rembrandt Hotel

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THE ART AND SCIENCE OF PATENT SEARCHING

Date/Time
Date(s) - To Be Confirmed

Price: £0.00 (ALL UK EVENTS ARE SUBJECT TO VAT)

Conference Ref: H9-3315

Brochure Download:

THE ART AND SCIENCE OF PATENT SEARCHING

Full details for the Art and Science of Patent Searching meeting which is to be held in Autumn 2015 will be posted in due course.  In the meantime if you have any queries please click here to contact Josephine Leak

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COMMON TECHNICAL DOSSIER

Date/Time
Date(s) - To Be Confirmed

Price: £0.00 (ALL UK EVENTS ARE SUBJECT TO VAT)

Conference Ref: A12-1115

Brochure Download:

COMMON TECHNICAL DOSSIER

Project Management/Collection of Critical Documents for Chemistry, Manufacturing and Control (CMC) for Global Registration (CTD) & Incorporate Quality by Design within the CTD

DETAILS OF VENUE, COST AND THE BROCHURE DOWNLOAD WILL BE AVAILABLE IN DUE COURSE.

INTRODUCTION
This 2-day Common Technical Dossier course will provide you with a clear understanding of the regulatory and technical requirements for CMC management of your full and generic application in major markets of EU and USA. Furthermore, the course examines the requirements for Global roll out of the dossier to ROW regions including, LATAM, ASEAN, MENA and CIS territories.
You will increase your ability to manage all aspects of development of the CMC aspects of applications after two days of intensive lectures, group work, and discussion sessions, covering everything you need to know about compiling the chemistry and pharmacy section of your generic dossier.

THIS COURSE WILL COVER THE FOLLOWING TOPICS

  • Development, analytical, formulation and quality experts to contribute to the effective compilation of CTD and allow effective review of documentation requiring agreement by regulators
  • Drive full understanding of Quality by Design, Critical Attributes and developing new products using the CQA Pyramid model
  • Compile and submit Module 3 (CTD) of your registration dossier
  • Identify development needs for applications taking a ‘right first time’ development approach and utilizing QBD
  • Identify extent of content expected by EU and US regulators
  • Provide practical experience and examples
  • Achieve the quickest turnaround of your submission
  • Deal effectively with your internal and external clients
  • Manage the Pharmaceutical Development and Quality aspects of your developments and registration dossier in Europe and US
  • Ensure all data needed has been collected in efficient manner
  • Ensure right first time development
  • Meet the legal framework and guidelines for the CMC/Quality part of the dossier, and links to GMP
  • Incorporate Quality By Design into your developments

WHO SHOULD ATTEND

  • Senior Analytical Chemists
  • Formulation Chemists
  • Technical Services Chemists
  • Registration staff (all levels)
  • Quality Managers
  • Quality Control Directors
  • R & D Project Managers

Trainer: Andrew Willis BSc.(Hons), MTOPRA – Independent Consultant in Advanced Regulatory Affairs and Pharmaceutical Development

If you have any queries please click here

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BASIC PHARMACOVIGILANCE

Date/Time
Date(s) - To Be Confirmed

Price: £0.00 (ALL UK EVENTS ARE SUBJECT TO VAT)

Conference Ref: A12-1015

Brochure Download:

BASIC PHARMACOVIGILANCE

Details of this 3 day meeting in December will be posted in due course, in the meantime, if you have any queries please click here.

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ABRIDGED APPLICATIONS

Date/Time
Date(s) - To Be Confirmed

Price: £0.00 (ALL UK EVENTS ARE SUBJECT TO VAT)

Conference Ref: A10-1015

Brochure Download:

ABRIDGED APPLICATIONS

Full meeting details will be posted in due course , in the meantime if you have any queries please click here

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