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gxpsystems.com

GXP Systems

GxP Systems, a leader in compliance and validation services, enables medical device, biotechnical and pharmaceutical clients to systematically and continuously lower the cost of compliance within their discovery, manufacturing, and supply chain facilities, without compromising compliance or quality.

http://www.gxpsystems.com/

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CONTACTS AT GXPSYSTEMS.COM

GXP SYSTEMS

LINDA MELLERICK

UN●●1H

THE●●●IUM

BLA●●●OOL , CO. CORK, 00000

IE

3532●●●●5050
LI●●●●●●●●●●●●●@GXPSYSTEMS.COM

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GXP SYSTEMS

LINDA MELLERICK

UN●●1H

THE●●●IUM

BLA●●●OOL , CO. CORK, 00000

IE

3532●●●●5050
LI●●●●●●●●●●●●●@GXPSYSTEMS.COM

View this contact

GXP SYSTEMS

LINDA MELLERICK

UN●●1H

THE●●●IUM

BLA●●●OOL , CO. CORK, 00000

IE

3532●●●●5050
LI●●●●●●●●●●●●●@GXPSYSTEMS.COM

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PAGE TITLE
GXP Systems | gxpsystems.com Reviews
<META>
DESCRIPTION
GxP Systems, a leader in compliance and validation services, enables medical device, biotechnical and pharmaceutical clients to systematically and continuously lower the cost of compliance within their discovery, manufacturing, and supply chain facilities, without compromising compliance or quality.
<META>
KEYWORDS
1 GxP
2 GxP Systems
3 Validation
4 Business competitiveness
5 Business efficiency
6 Compliance costs
7 Compliance systems
8 Life science manufacturers
9 Life science manufacturing
10 Managed services
CONTENT
Page content here
KEYWORDS ON
PAGE
stericycle gxp workforce,stericycle gxp solutions
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utf-8
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GXP Systems | gxpsystems.com Reviews

https://gxpsystems.com

GxP Systems, a leader in compliance and validation services, enables medical device, biotechnical and pharmaceutical clients to systematically and continuously lower the cost of compliance within their discovery, manufacturing, and supply chain facilities, without compromising compliance or quality.

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1

GXP Systems

http://www.gxpsystems.com/services-serialization.html

We can create a solution for your entire serialization program. Since coming into law, the Directive 2011/62/EC of 8 June 2011 - which amended Directive 2001/83/EC on the Community Code Relating to Medicinal Products for Human Use as regards to the prevention of the entry into the legal supply chain of falsified medicinal products - makes it the responsibility of each pharmaceutical company to ensure that the implemented serialization system is fully compliant with this regulation. Phone: 353 21 4215 050.

2

GXP Systems

http://www.gxpsystems.com/services-quality.html

Our approach delivers a compliant quality program as well as introducing various quality improvement initiatives. Stericycle GxP Solutions highly experienced team of quality experts develops, rolls out and maintains the Quality Management Systems required for the organizational structures, procedures, processes and resources to implement quality management at our customers manufacturing sites. We provide in-depth knowledge and expertise from dealing with different quality standards. Phone: 353 21 4215 050.

3

GXP Systems

http://www.gxpsystems.com/services-remediation.html

You will benefit from our proven approach to Remediation. If you’ve received a warning letter or consent decree, it’s a relief to know that expert help is just a. Phone call away. With in-depth knowledge of regulatory guidelines and our superior ability to return systems to a state of validated compliance, we excel at remediation services. We offer a complete range of remediation services, focusing on improving your operations and. Comprehensive Objectives and Priority Definition. Internal reporting and ...

4

GXP Systems

http://www.gxpsystems.com/services-validation.html

Our extensive range of validation services will meet your unique needs. Stericycle GxP Solutions has a successful track record of introducing a right-sized validation approach to our life science customers. Whether it is introducing a new product, transferring a line, or bringing an existing line into a state of validation, our expert validation teams will provide you with up-to-date policies and procedures. You will benefit from our right-sized validation approach. Assessment of policies and procedures.

5

GXP Systems

http://www.gxpsystems.com/news.html

GxP Systems becomes Stericycle GxP Solutions. Tuesday, May 10, 2016. Cork, Ireland  May 10th, 2016 Stericycle GxP Solutions, a leader in compliance and validation services, today announced that GxP Systems has officially changed its name to Stericycle GxP Solutions. GxP Systems has been a. Cork, Ireland May 10th, 2016. The Company also announced the creation of Stericycle GxP Workforce which will focus on helping life science organizations build strong and effective teams around the globe. The creation o...

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Skip to main content. 2016 Sponsors and Exhibitors. 2016 Sponsors and Exhibitors. Earlybird tickets have just gone on sale. Register now! Sign up for our newsletter. Speakers announced for 2017 include:. Speaker applications are now open! Apply to speak at our 2017 event. About Global Expansion Summit. Global Expansion Summit is the leading global event on international expansion and doing business across borders in the era of innovation and technological transformation. View all sponsors and exhibitors.

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GXPSYS Inc. | Best Validation & Regulatory Compliance services | Project Management

FRIDAY, April 18, 2011 12:00. Welcome to GXPSYS Inc. GXPSYS provides validation and compliance consulting services and industry specific products to the Pharmaceutical and Biotech industries. We provide expansive guidance and expertise in areas including quality systems, computer and equipment validation, automated process systems, commissioning and qualification of new and existing facilities, manufacturing and lab equipment systems. Our goal is to remain the industry leader in providing excelle...

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GXP Systems

Helping life science organizations build strong and effective teams. Providing expert Regulatory Compliance solutions.

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GxP Systems | The Regulatory Compliance Experts

The Regulatory Compliance Experts. Repackaging of Certain Human Drug Products by Pharmacies and Outsourcing Facilities. November 4, 2015. In February 2015, the US FDA released a draft guidance on the repackaging of certain products by pharmacies and outsourcing facilities. The closing date for comment was set for 17.05.2015, but when the actual guidance is expected to be implemented is still to be confirmed. No more than 14 days beyond completion of the sterility test or 28 days from the time of repackag...

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