Similar sites like 515-consulting.com

Products and Services for Regulatory Publishing Activities - 515 Consulting Group

e-Regulatory and e-submission publishing and solutions

Categories: Software/Hardware, Personal Websites and Blogs
Topics: 510k, 515 consulting group, ctd, ectd, esubmission, fda, lee knoch, products and services for regulatory publishing activities, publishing, regulatory, submission, templates

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Sites similar to 515-consulting.com - Top 29 515-consulting.com alternatives

510k.org
510k, FDA 510(k), UL, CCC Mark, CE Mark, CE Marking - Wellkang® LLC - world leading regulatory consultancy
Wellkang LLC - world leading regulatory consultancy in FDA 510(k), UL, CCC Mark, CE Mark, CE Marking.

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master-resale-rights.com
Private Label Rights (PLR), Master Resale Rights, Resell Rights, Private Label Right, PLR eBook, Video, PLR Articles. Largest Catalog.
Since 1999 - Private Label Rights, Master Resell Rights, Master Resale Rights and Private Label Rights to Thousands of eBooks, Software, PLR Videos, Audio Books,Resale Graphics, and More, Complete with Private Label Rights and Master Resell Rights. World's Largest Catalog, by far! Over 10,000 resale products.

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Categories: Recreation/Travel, Computers/Multimedia, Health/Alternative, Online Shopping, Shopping

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web-consulting-services.com
Search Engine Optimization, Web Design, Graphics and Photography in Charlotte NC - Web Consulting Services
Web Consulting Services and Iconstructwebs offers website design and hosting in the Carolinas and servicing most of the southeastern states.

Categories: Internet Services, Information Technology

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fdacg.com
FDA Compliance Consultants | FDA Consultant | FDA Consulting Services | FDA 483
We can help you achieve and maintain full FDA compliance! We are former FDA employees, and we have decades of regulatory experience in dietary supplements, medical devices, drugs, and more.

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horn-pharma.de
Horn Pharmaceutical Consulting - ASMF, Active Substance Master File, US-DMF, Drug Master File, Certificate of suitability, CEP, CTA ,Clinical Trial Application, IND, Investigational New Drug Application, CTD, Common Technical Document, European MAA, Marketing Authorization Application, NDA, New Drug Application / BLA, Biologic License Application, SPCs, Summary of Product Characteristics, clinical or nonclinical study protocols and reports, clinical or nonclinical summaries and overviews, qualit
HORN Pharmaceutical Consulting provides regulatory and business advice to companies from the pharmaceutical, biotechnology and medical device industries.

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biotechnologylawgroup.com
Patent Attorneys, FDA Regulatory, Technology Transactions | San Diego, Irvine, Los Angeles | Torrey Pines Law Group®
Patent attorneys, FDA regulatory advisors, and technology transactions lawyers having biotech, pharmaceutical, medical device, and artificial intelligence (AI) experience. The firm's intellectual property attorneys focus on helping you develop, enforce, and commercialize life sciences and healthcare technologies internationally. The firm's regulatory advisors focus on navigating the process of obtaining international drug and medical device approvals and clearances. Our business attorneys and business advisors focus on making deals and closing technology transactions worldwide.

Categories: Business, Government and Legal Organizations

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aquamarinegroup.com
Welcome to The AquaMarine Group, Inc.
Since 1996, The AquaMarine Group, Inc.’s services have been sought and retained by pharmaceutical firms, to furnish expertise in the areas of regulatory review, application writing, cGMP compliance/mock pre-approval audit services, R&D portfolio analysis, contracted management services, and new product/technology evaluation and promotion. Services furnished to clients include not only review and commentary, but have also included project management for a number of significant filings.

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fda-registration.com
FDA Registration & US Agent Service for non-US manufacturers of pharmaceutical and medical devices, foods and food products offered by Wellkang® LLC - FDAagent.us - FDA-Registration.com
FDA Registration & US Agent Service: FDA U.S. Agent services for non-US manufacturers of pharmaceutical and medical devices, foods and food products offered by Wellkang® LLC - FDAagent.us - FDA-Registration.com

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torreypineslaw.com
Torrey Pines Law Group® | Patent Attorneys | FDA Regulatory | Technology Transactions | San Diego
San Diego patent attorneys, FDA regulatory advisors, and technology transactions lawyers having biotechnology, pharmaceutical, medical device, diagnostics, precision medicine, and artificial intelligence (AI) experience.

Moz DA: 19 Moz Rank: 3.1 Semrush Rank: 2,120,053 Facebook ♡: 1,262
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softconf.com
The Softconf/START Conference Manager
The Softconf/START Conference Manager, a software for managing the conference submission and review process

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viglya.com
Viglya: promoting science, honoring life - promoting science, honoring life
Viglya provides a broad spectrum of drug safety services tailored to... Included are some links we hope will serve as references and ... Viglya’s commitment to its team and stakeholders includes...

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weballey.nl
WEBalley - web publishing voor beginners
HTML tutorials en web design gidsen. Gratis templates om beginners te helpen met het maken van hun eerste home page. Tips over hoe graphics te gebruiken op je website. Tutorials die je alles vertellen wat je weten moet om je eerste website te maken en te publiceren op het web. Online home page wizard, aanmelden bij zoekmachines, web design resources, nieuws headlines.

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rapidmicromethods.com
Rapid Microbiology and Rapid Microbiological Methods
Welcome to the most comprehensive, educational online resource for rapid microbiology technologies, regulatory policies, validation strategies, current trends, expert training and consulting.

Categories: Blogs/Wiki, Reference

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zeincro.com
ZEINCRO : CRO - Contract Services Organisation
ZEINCRO is a contract research organisation (CRO) specialist in Central- and South-Eastern Europe.

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esc-berlin.com
Snickartjänster, renovering och ombyggnation

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newfound.org
Home - Newfound
• An Inquiry of Place Newfound is a nonprofit publisher whose celebrated work investigates how place shapes identity, imagination, and understanding through print and digital publications and events.

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Categories: Education/Reference, Domain Parking

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newfoundjournal.org
Newfound | An Inquiry of Place
Newfound is a nonprofit publisher based in Austin, Texas. Our work explores how place shapes identity, imagination, and understanding. The journal is published tri-annually and features fiction, poetry, nonfiction, visual arts, reviews, and more. We also publish poetry chapbooks through our annual Gloria E. Anzaldúa Poetry Prize.

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axys-network.com
AXYS-NETWORK-Pharmaceutical consulting firm
Axys-network is a pharmaceutical consulting firm specializing in aseptic processes and in Transition Management - Manufacturing, Quality, Regulatory. Remediation experts for troubleshooting and continuous improvement

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globalvetlink.com
GVL | GVL assists in animal safety through simplifying compliance with animal movement requirements and Animal Disease Traceability.
GVL provides online animal health software solutions for veterinarians for digital Veterinary Feed Directives (VFDs), health certificates (certificates of veterinary inspection or CVIs), veterinary prescriptions (scripts), Equine Infectious Anemia (EIA) or Coggins tests and GoPass Equine Passports (6-month health certificates).

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Categories: Marketing/Merchandising, Reference

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ectdoffice.com

eCTD Office - eCTD (NeeS / VNeeS) Publishing Software Solution

Mono eCTD Office is a suite of integrated NeeS / eCTD software products for the validation, creation, viewing, manipulation and archiving of NeeS / eCTD submissions of regulatory documentation by pharmaceutical companies to the regulatory authorities.

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thoughtcollection.org
Expanding Perspectives
We produce nonfiction publications that expand perspectives.

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myvetlink.com
MyVetLink Owner Account and App | GVL
MyVetLINK gives animal owners and producers instant online access to Veterinary Feed Directives (VFDs), veterinary prescriptions (scripts), Certificates of Veterinary Inspection (CVIs) or health certificates, Equine Infectious Anemia (EIA or Coggins) test certificates and GoPass® Equine Passports (6-month health certificates).

Moz DA: 19 Moz Rank: 2.5 Facebook ♡: 207
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pharmaqm.com
PharmaQM
Pharmaceutical regulatory consultancy services from a former UK Pharmaceutical Assessor and EDQM Rapporteur, former EMEA Expert and current WHO Quality Assessor. Regulatory strategy, advice, dossier review and gap analysis, training Procedural advice and liaison with regulatory authorities

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opulus.com
Opulus, Portal for the Pharmaceutical Industry
opulus, endotoxin, LAL, 21 CFR Part 11, database, warning letter, regulatory, competency, pharmaceutical, biotechnology, forum, validation, inspection, fda, drug, pipetta, research, cactus, software, pyrodoq, pyrosolution, equ, equant, dissolution, competency, training, sop, e-learning, on-line, online, quartz crystal microbalance, qcm, tsm, thickness shear

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regulatory.com.ua
Patern Ltd. | Regulatory Affairs Outsourcing ft Pattern of USA Inc. Homepage, FAQ
510(k) – Premarket Notification for Medical Device aka PMN
AADA – Abbreviated antibiotic drug application
ACTD – ASEAN common technical dossier
ADR – Adverse drug reaction
AE – Adverse event
AIM – Active ingredient manufacturer
AIMD – Active implantable medical device
ANDA – Abbreviated new drug application
API – Active pharmaceutical ingredient
AR – Assessment Report (European Union)
ASMF – Active Substance Master File
ATMPs – Advanced therapy medicinal products
BA – Bioavailability
BAP – Biotechnology Action Program
BIND – Biological investigational new drug
BLA - Biologic License Application
BWP – Biotech Working Party (EMA)
C&P – Chemistry and Pharmacy
CA – Competent authority
CANDA – Computer assisted new drug application
CAP – Centrally authorized product
CAPA – Corrective action and preventive action
CAPLA – Computer Assisted Product License Application
CCDS – Company core data sheet
CD – Controlled drug
CDSCO – Central Drug Standard Organization (India)
cGLP – Current good laboratory practice
cGMP – Current good manufacturing practice
Cl – Total body clearance
CLO – Clinical overview
CLS – Clinical summary
CMC – Chemistry – manufacturing – controls
CMP – Certificate of Medicinal Product
COA – Certificate of analysis
CoFS – Certificate of Free Sale
CP – Centralized procedure (European Union)
CP – Comparability protocol (USA)
CPP – Certificate of pharmaceutical product
CQA – Clinical quality assurance
CR – Controlled release
CRO – Clinical Research Organization
CSI – Core safety information
CSP – Core safety profile
CSR – Clinical study report (European Union)
CT – Clinical trial
CTA – Clinical trial application
CTA – Clinical trial authorization
CTD – Clinical Trials Directive
CTD – Common technical document/dossier
CTMS – Clinical trial management system
CTS – Common technical specification
CVM – Center for Veterinary Medicine (US)
DACS – Detailed and critical summary
DAE – Discontinuation due to an a

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duvalfdalaw.com
DuVal & Associates - FDA Law
DuVal & Associates is a boutique law firm located in Minneapolis, Minnesota. We offer game-changing guidance for achieving successful outcomes in highly-regulated markets. Our clientele includes companies that manufacture and/or market pharmaceuticals, medical devices, biologics, nutritional/dietary supplements and foods.

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Categories: Business, Government and Legal Organizations

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issr-journals.org
ISSR Journals
ISSR Journals

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Categories: Entertainment, Education

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cimbal.net
Walter Cimbal || BFF Fotodesign
Walter Cimbal || BFF Fotodesign

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judyburton.com
Advena USA FDA Regulatory Consultants
Home page for Advena USA FDA Regulatory Affairs Consultants

Categories: Business, Business

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