|
FDA.COM
is an internet communications media site which provides
in-depth, authoritative health and medical resources for those
seeking credible validated Food, Drug and Regulatory Compliance
information. With millions of unique visitors every week,
FDA.COM is the most comprehensive, trusted and heavily
trafficked source in the food, pharmaceutical and biotechnology
industry.
FDA.COM provides only the relevant information in an easy to
navigate portal format, providing quick access links to critical
Food, Drug, Biotechnology, Device and Cosmetic regulatory
information and US FDA streamlined links. Portal information
cites credible sources such as CDC, NIH, FDA, CDER, CBER, CDRH,
CVM, ORA and other federal agencies.
FDA.COM
provides an exceptional Portal focusing on credible information
for disease and condition states utilizing open dialog and the
sharing of professional information, delivering immediate
streamlined quality information to consumers, healthcare
professionals, pharmaceutical and biotechnology industry.
FDA.COM, owned and operated by GMP Publications Inc. GMP
Publications clients include most of the top biopharmaceutical,
medical device, food, nutraceutical and cosmetic firms in the
world.
FDA.COM delivers results:
-
Consumer resource which provides credible information that
drives consumers to FDA.COM
-
1.8 Million page views weekly
-
With no advertising effort, FDA.COM has search engine
optimization and credibility – consistently No. 3-5 on Yahoo
and Google lists for “FDA” searches for the past 8 years
-
Option for vendor ads for individual condition specific
sites, also featuring category exclusivity
-
30% of our audience is comprised of Bio-Pharmaceutical and
Life Science professionals who spend an aggregate of $3.3
billion per year on goods and services industry wide
-
Additional network distribution advertising opportunities
available
o
The GXPNews
e-newsletter circulated to over 160,000 professional subscribers
o
GMP Publications are
carried by Millions worldwide
Everyone seeking information pertaining to the “FDA” finds us!
Get global exposure with FDA.COM today.
Contact:
-
GMP Publications, Inc. is the world's leader in Federal
Regulations with over 7500 customers world-wide!
-
FDA.COM is the most heavily trafficked site in the industry.
1.8 Million page views per week.
-
GXPNews e-newsletter circulated to over 160,000
professionals subscribers every Month.
-
30% of our audience is comprised of Bio-Pharmaceutical and
life scientist professionals who spend an aggregate of $3.3
billion dollars per year on goods and services
industry-wide.
-
Over 60% of our users forward our services, booklets and
newsletter content to others.
-
FDA.COM (Owned and Operated by GMP Publications, Inc.)
FDA.COM discussion forums provides a portal type of forum
focusing on open dialog and the sharing of professional
information through an interactive discussion group environments
and direct Questions and Answers (Q&A) responses, delivering
immediate streamlined quality information to the industry
professionals, by industry leaders (known as Sponsors)
And at the same time allowing industry leaders to promote
services and products.
Sponsors are Vendors, Contractors or Professional Services
firms, who field technical and compliance issues by the
industry. Sponsors currently enjoy the exclusivity of their
field or technology sector and by assisting the industry,
enables them to stand out as the authoritarian leader of that
industry.
FDA.COM is the 'next step', taking industry professionals and
visitors beyond FDA.GOV or the Food and Drug Administration
Department. Where the Food and Drug Administration provides the
regulations that creates the Laws that Pharmaceuticals,
Biotechnology and other Regulated Industry must abide to, they
lack in discussing or guiding the industry of the 'How' and
'Why' needed to comply.
FDA.COM is the 'next step', allowing industry to talk to
industry concerning the 'How' and 'Why' of conformity and
compliance concerning issues from every facet of the industry.
The Food and Drug Administration informs regulated industry that
they must conform to 21 CFR Parts xxx, however, they don't tell
industry how to comply or what is required to meet the
regulations. Whether GMP, GCP, GLP, Validation, Clinical,
Biotechnology, or other regulated industry, the FDA leaves it up
to industry to decide the 'how' and then to implement, as they
should.
Industry must learn, and FDA.COM provides the forum for
learning!
Have Money Making Ideas? FDA.COM has the audience!
FDA.COM is currently seeking to expand it's services and
information portal lines and operations. FDA.COM is seeking
affiliations, ideas, suggestions, venture capital, partnerships
and/or strategic alliances with established firms and companies
looking to become part of the FDA.COM On-line Information Portal
family.
Contact Information:
Mailing Address:
P.O. Box 335
Medford, NJ 08055 |
Physical Address:
4 Linda Lane, Unit B
Southampton, NJ 08088 |
For
information, please call 1-866-544-9001or 856-810-1825 and ask
for Michael Van Horn, Director of Sales and Marketing, FDA.COM.
For Regulatory Information contact John Cuspilich Director
Regulatory Affairs at 856-810-7331. |
