ArisGlobal

ArisGlobal Events

Sep
23
Tue
IDMP Forum 2014 – Boston, MA @ Courtyard Boston Cambridge
Sep 23 @ 09:00 – 12:00

*Registration from 8:30AM-9:00AM

This half day IDMP Forum will take us to Boston, Massachusetts. Courtyard Boston Cambridge is conveniently located among hotels near Harvard and boasts of quick access to the city’s top dining & attractions.

Key Session abstracts

IDMP, A Global Challenge and Opportunity – Wim Cypers
The European Commission has mandated that by 2016 companies will need to submit product information according to the ISO-IDMP standard. This is however not only a European challenge, the FDA is very much working on the adoption of the IDMP standard and it is only a matter of time before this will also become mandatory. In this session we will be presenting:
– regulatory basis for the standard and what companies will need to comply to and how they could approach this challenge
– have a detailed look at the different standard that make up ISO-IDMP
– based on some examples understanding the structure and elements of the ISO-IDMP dictionary
– have a look at the opportunities that adopting the standard can mean for your company beyond compliance

Preparing for IDMP – Pratyusha Pallavi
The benefits of implementing IDMP within your organization can be tremendous. However ensuring that your organization is ready to face the IDMP challenge will require a close cooperation between multiple departments within your organization. Where can the data be found ? Is a cleanup of the data required ? Are the appropriate processes in place to continue to benefit from a central repository ? are only a few questions that need to be addressed. In this session we will present a step wise approach that will address these and other questions and that will ensure that your organization takes a logical approach to the compliance challenge as well as ensure that you can ensure the efficiency gains that the IDMP standard can bring to your organization.

Boston

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Sep
24
Wed
IDMP Forum 2014 – Chicago, IL @ Fairfield Inn & Suites Chicago Downtown/River North
Sep 24 @ 09:00 – 12:00

*Registration from 8:30AM-9:00AM

The third stop of our IDMP Forum takes us to Chicago, Illinois. The Fairfield Inn & Suites Chicago Downtown/River North offers free upgraded Wi-Fi throughout hotel and 2,000 sq. ft. of shared meeting space.

Key Session abstracts

IDMP, A Global Challenge and Opportunity – Wim Cypers
The European Commission has mandated that by 2016 companies will need to submit product information according to the ISO-IDMP standard. This is however not only a European challenge, the FDA is very much working on the adoption of the IDMP standard and it is only a matter of time before this will also become mandatory. In this session we will be presenting:
– regulatory basis for the standard and what companies will need to comply to and how they could approach this challenge
– have a detailed look at the different standard that make up ISO-IDMP
– based on some examples understanding the structure and elements of the ISO-IDMP dictionary
– have a look at the opportunities that adopting the standard can mean for your company beyond compliance

Preparing for IDMP – Pratyusha Pallavi
The benefits of implementing IDMP within your organization can be tremendous. However ensuring that your organization is ready to face the IDMP challenge will require a close cooperation between multiple departments within your organization. Where can the data be found ? Is a cleanup of the data required ? Are the appropriate processes in place to continue to benefit from a central repository ? are only a few questions that need to be addressed. In this session we will present a step wise approach that will address these and other questions and that will ensure that your organization takes a logical approach to the compliance challenge as well as ensure that you can ensure the efficiency gains that the IDMP standard can bring to your organization.

chicago

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Sep
25
Thu
IDMP Forum 2014 – San Francisco, CA @ San Francisco Marriott Marquis
Sep 25 @ 09:00 – 12:00

*Registration from 8:30AM-9:00AM

The fourth and final stop of the ArisGlobal IDMP Forum takes us to the San Francisco Marriott Marquis located in San Francisco, CA. Discover this historic site, located steps from the Moscone Center, Union Square and other top attractions in San Francisco.

Key Session abstracts

IDMP, A Global Challenge and Opportunity – Wim Cypers
The European Commission has mandated that by 2016 companies will need to submit product information according to the ISO-IDMP standard. This is however not only a European challenge, the FDA is very much working on the adoption of the IDMP standard and it is only a matter of time before this will also become mandatory. In this session we will be presenting:
– regulatory basis for the standard and what companies will need to comply to and how they could approach this challenge
– have a detailed look at the different standard that make up ISO-IDMP
– based on some examples understanding the structure and elements of the ISO-IDMP dictionary
– have a look at the opportunities that adopting the standard can mean for your company beyond compliance

Preparing for IDMP – Pratyusha Pallavi
The benefits of implementing IDMP within your organization can be tremendous. However ensuring that your organization is ready to face the IDMP challenge will require a close cooperation between multiple departments within your organization. Where can the data be found ? Is a cleanup of the data required ? Are the appropriate processes in place to continue to benefit from a central repository ? are only a few questions that need to be addressed. In this session we will present a step wise approach that will address these and other questions and that will ensure that your organization takes a logical approach to the compliance challenge as well as ensure that you can ensure the efficiency gains that the IDMP standard can bring to your organization.

francisco

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Sep
27
Sat
RAPS Regulatory Convergence Conference @ Austin Convention Centre
Sep 27 – Oct 1 all-day
Sep
30
Tue
IDMP Forum 2014 – London @ London, UK
Sep 30 @ 09:00 – 12:00

*Registration from 8:30AM-9:00AM

Venue to be confirmed shortly.

Key Session abstracts

IDMP, A Global Challenge and Opportunity – Wim Cypers
The European Commission has mandated that by 2016 companies will need to submit product information according to the ISO-IDMP standard. This is however not only a European challenge, the FDA is very much working on the adoption of the IDMP standard and it is only a matter of time before this will also become mandatory. In this session we will be presenting:
– regulatory basis for the standard and what companies will need to comply to and how they could approach this challenge
– have a detailed look at the different standard that make up ISO-IDMP
– based on some examples understanding the structure and elements of the ISO-IDMP dictionary
– have a look at the opportunities that adopting the standard can mean for your company beyond compliance

Preparing for IDMP – Pratyusha Pallavi
The benefits of implementing IDMP within your organization can be tremendous. However ensuring that your organization is ready to face the IDMP challenge will require a close cooperation between multiple departments within your organization. Where can the data be found ? Is a cleanup of the data required ? Are the appropriate processes in place to continue to benefit from a central repository ? are only a few questions that need to be addressed. In this session we will present a step wise approach that will address these and other questions and that will ensure that your organization takes a logical approach to the compliance challenge as well as ensure that you can ensure the efficiency gains that the IDMP standard can bring to your organization.


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Click here to view IDMP Forum 2014 (US)

Oct
2
Thu
IDMP Forum 2014 – Frankfurt @ Frankfurt, Germany
Oct 2 @ 09:00 – 12:00

*Registration from 8:30AM-9:00AM

Venue to be confirmed shortly.

Key Session abstracts

IDMP, A Global Challenge and Opportunity – Wim Cypers
The European Commission has mandated that by 2016 companies will need to submit product information according to the ISO-IDMP standard. This is however not only a European challenge, the FDA is very much working on the adoption of the IDMP standard and it is only a matter of time before this will also become mandatory. In this session we will be presenting:
– regulatory basis for the standard and what companies will need to comply to and how they could approach this challenge
– have a detailed look at the different standard that make up ISO-IDMP
– based on some examples understanding the structure and elements of the ISO-IDMP dictionary
– have a look at the opportunities that adopting the standard can mean for your company beyond compliance

Preparing for IDMP – Pratyusha Pallavi
The benefits of implementing IDMP within your organization can be tremendous. However ensuring that your organization is ready to face the IDMP challenge will require a close cooperation between multiple departments within your organization. Where can the data be found ? Is a cleanup of the data required ? Are the appropriate processes in place to continue to benefit from a central repository ? are only a few questions that need to be addressed. In this session we will present a step wise approach that will address these and other questions and that will ensure that your organization takes a logical approach to the compliance challenge as well as ensure that you can ensure the efficiency gains that the IDMP standard can bring to your organization.


Please fill the form below to register for the event.
 

* denotes required field




Click here to view IDMP Forum 2014 (US)

Oct
4
Sat
IDMP Forum 2014 – Basel @ Basel, Switzerland
Oct 4 @ 09:00 – 12:00

*Registration from 8:30AM-9:00AM

Venue to be confirmed shortly.

Key Session abstracts

IDMP, A Global Challenge and Opportunity – Wim Cypers
The European Commission has mandated that by 2016 companies will need to submit product information according to the ISO-IDMP standard. This is however not only a European challenge, the FDA is very much working on the adoption of the IDMP standard and it is only a matter of time before this will also become mandatory. In this session we will be presenting:
– regulatory basis for the standard and what companies will need to comply to and how they could approach this challenge
– have a detailed look at the different standard that make up ISO-IDMP
– based on some examples understanding the structure and elements of the ISO-IDMP dictionary
– have a look at the opportunities that adopting the standard can mean for your company beyond compliance

Preparing for IDMP – Pratyusha Pallavi
The benefits of implementing IDMP within your organization can be tremendous. However ensuring that your organization is ready to face the IDMP challenge will require a close cooperation between multiple departments within your organization. Where can the data be found ? Is a cleanup of the data required ? Are the appropriate processes in place to continue to benefit from a central repository ? are only a few questions that need to be addressed. In this session we will present a step wise approach that will address these and other questions and that will ensure that your organization takes a logical approach to the compliance challenge as well as ensure that you can ensure the efficiency gains that the IDMP standard can bring to your organization.


Please fill the form below to register for the event.
 

* denotes required field




Click here to view IDMP Forum 2014 (US)

Oct
6
Mon
IDMP Forum 2014 – Paris @ Paris, France
Oct 6 @ 09:00 – 12:00

*Registration from 8:30AM-9:00AM

Venue to be confirmed shortly.

Key Session abstracts

IDMP, A Global Challenge and Opportunity – Wim Cypers
The European Commission has mandated that by 2016 companies will need to submit product information according to the ISO-IDMP standard. This is however not only a European challenge, the FDA is very much working on the adoption of the IDMP standard and it is only a matter of time before this will also become mandatory. In this session we will be presenting:
– regulatory basis for the standard and what companies will need to comply to and how they could approach this challenge
– have a detailed look at the different standard that make up ISO-IDMP
– based on some examples understanding the structure and elements of the ISO-IDMP dictionary
– have a look at the opportunities that adopting the standard can mean for your company beyond compliance

Preparing for IDMP – Pratyusha Pallavi
The benefits of implementing IDMP within your organization can be tremendous. However ensuring that your organization is ready to face the IDMP challenge will require a close cooperation between multiple departments within your organization. Where can the data be found ? Is a cleanup of the data required ? Are the appropriate processes in place to continue to benefit from a central repository ? are only a few questions that need to be addressed. In this session we will present a step wise approach that will address these and other questions and that will ensure that your organization takes a logical approach to the compliance challenge as well as ensure that you can ensure the efficiency gains that the IDMP standard can bring to your organization.


Please fill the form below to register for the event.
 

* denotes required field




Click here to view IDMP Forum 2014 (US)

Oct
15
Wed
TOPRA Annual Symposium @ The Square, Brussels. Mont des Arts
Oct 15 – Oct 17 all-day
Feb
19
Thu
IDMP 101 – An overview of IDMP
Feb 19 @ 10:00 – 11:00

As a Pharma company you must aware of the upcoming IDMP guidelines which will come into force in 2016.

This is however not just a European challenge, the FDA is also working on the adoption of the IDMP and so are the regulators in Japan.

Is your organization ready for IDMP? As a pharmaceutical company you may be tempted to look at IDMP as an additional standard that needs to be complied with, or as an effort requiring additional resources. You may also think that the ownership of IDMP lies with the regulatory function in your organization. While this is true to a certain extent we must remember that the sources of data for IDMP will lie outside and will involve intense collaboration between departments such as regulatory, safety, manufacturing to name a few.

Join us for this webinar on ‘IDMP 101- An overview of IDMP’ and gain insights into

a. The regulatory background
b. The definition of IDMP
c. The key terms within IDMP
d. The Impact on other divisions of your organization
e. IDMP implementation Challenges
f. The Logical approach to IDMP

Event Details:
Webinar: IDMP 101- An overview of IDMP
Date: 19th February 2015
Time: 12.00 PM GMT or 7 AM Eastern

Click the link below to register

Register Now