Personal Information
Industry
Consulting / Advisory
Website
www.3-14.com
About
pi is the strategic partner of choice to some of the world’s leading life science companies. We offer our clients unique expertise and strategic consultancy of the highest quality.
We dedicate ourselves to bringing excellence to the life sciences industry.
We’ve grown by learning how to be better.
Better resourced to focus our faculty of consultants’ singular experience and knowledge.
Better managed to share their depth of understanding.
Better prepared to challenge orthodox thinking.
And better able to redefine accepted best practice.
To accept no other standard than excellence.
Tags
life science industry
life science
pharma
life sciences consultancy
pharmaceutical industry
life sciences industry
fda
pharmaceutical
european union
medical devices
european legislation
healthcare
medical device regulations
regulatory compliance
data integrity
general data protection regulation
ema
gdpr
gmp
medical device directive
pi life sciences consultancy
data legislation
data privacy
big data
quality metrics program
data
data security
usp
compliance
ispe
european medical device regulations
manufacturing
pharmacovigilance
analytical instrument qualification
elemental impurities
aiq
good manufacturing practices
healthcare consulting
pi
data law
international law
samd
software as a medical device
medical software
regulatory affaires
regulatory
performance qualification
operational qualification
installation qualification
pharmacopeia
nir
infrared spectroscopy
near-infrared spectroscopy
instrument qualifiation
ich q2: validation of analytical procedures
analytical procedure transfer
analytical procedure verification
analytical procedure validation
analytical lifecycle
analytical target profile
automation
continuous manufacturing
patient centered healthcare
patient centred healthcare
internet of things
personal data
europe
instrument qualification
data quality
ich
ich q3d guideline
privacy by design
european commission
quality metrics
fdasia
vigilance
medical device vigilance
medicine
production
product quality assessment
who
signal detection
idmp
iso
result review
review process
review by exception
data audit
periodic review
audit trail review
data integrity compliance
soft skills
data integrity audit
data life cycle
data lifecycle
ivdr
eu
mhra
alcoa
strategic consultancy
consulting services
active implantable medical device directive
mdr
See more
Presentations
(17)Personal Information
Industry
Consulting / Advisory
Website
www.3-14.com
About
pi is the strategic partner of choice to some of the world’s leading life science companies. We offer our clients unique expertise and strategic consultancy of the highest quality.
We dedicate ourselves to bringing excellence to the life sciences industry.
We’ve grown by learning how to be better.
Better resourced to focus our faculty of consultants’ singular experience and knowledge.
Better managed to share their depth of understanding.
Better prepared to challenge orthodox thinking.
And better able to redefine accepted best practice.
To accept no other standard than excellence.
Tags
life science industry
life science
pharma
life sciences consultancy
pharmaceutical industry
life sciences industry
fda
pharmaceutical
european union
medical devices
european legislation
healthcare
medical device regulations
regulatory compliance
data integrity
general data protection regulation
ema
gdpr
gmp
medical device directive
pi life sciences consultancy
data legislation
data privacy
big data
quality metrics program
data
data security
usp
compliance
ispe
european medical device regulations
manufacturing
pharmacovigilance
analytical instrument qualification
elemental impurities
aiq
good manufacturing practices
healthcare consulting
pi
data law
international law
samd
software as a medical device
medical software
regulatory affaires
regulatory
performance qualification
operational qualification
installation qualification
pharmacopeia
nir
infrared spectroscopy
near-infrared spectroscopy
instrument qualifiation
ich q2: validation of analytical procedures
analytical procedure transfer
analytical procedure verification
analytical procedure validation
analytical lifecycle
analytical target profile
automation
continuous manufacturing
patient centered healthcare
patient centred healthcare
internet of things
personal data
europe
instrument qualification
data quality
ich
ich q3d guideline
privacy by design
european commission
quality metrics
fdasia
vigilance
medical device vigilance
medicine
production
product quality assessment
who
signal detection
idmp
iso
result review
review process
review by exception
data audit
periodic review
audit trail review
data integrity compliance
soft skills
data integrity audit
data life cycle
data lifecycle
ivdr
eu
mhra
alcoa
strategic consultancy
consulting services
active implantable medical device directive
mdr
See more