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Atop Pharma Solutions
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About original
Calculation of PDE and NOAEL
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Checkout
Checkout-Result
Cleaning Validation and MACO calculation
Contact original
Copyright Filing in India and USA
Copyright Infringement Strategy
Copyright Litigation
Copyright Opposition
Copyright TM-C certificate prosecution
Country-Specific Trademark Search
Deficiencies management
Design Filing in India and USA
Design Infringement Analysis
Design Litigation
Design patent filing in the USA
Donation Confirmation
Donation Failed
Donor Dashboard
Drafting and submission management of PSUR, PBRER, PADER, Clinical Overview and DSURs: Comprehensive Pharmacovigilance Service packages for ROW region
eCTD/NEES publication services
Establishment of PSMF and drafting of Risk management plan
FTO Report
Gap Analysis
Home
Home Page
Infringement Analysis Report
Legal Notice and Seizures
Lifecycle maintenance: variations (Type IA, IB, II), renewal, and MA transfer, ‘sunset clause’ exemptions package, withdrawal
Literature search -Global/local literature search and review for reports of adverse events for all types of products, using standard terms
Local regulatory support
MA duplication procedure
MAA dossier – review and compilation of modules 1 to 5
Monitoring of literature for aggregated reports and safety information
My account
Patent Drafting and Filing before Patent Registry
Patent Infringement Suits and Litigation
Patent Prior Art Search
Patents
PCT Application Filing
Pct National Phase Application Prosecution
Pharmacovigilance
Post Grant and Pre Grant-Oppositions
Preparation of Toxicology reports
Product information preparation – SPC, PIL and Labelling
Products
Readability Testing and Bridging report
Regulatory due diligence and strategy
Regulatory Services
Regulatory services for specific countries e.g. LATAM, CIS + ex members, ASEAN, South Africa, ANZ, Botswana, Switzerland, etc.
Sample Page
Scientific and medical writing: Drafting of Clinical/Non-clinical report or overview, narrative, IMPD with all regulatory compliance of EMA/any country
Shop
Signal detection
Toxicology
Trademark
Trademark Filing before various Trademark Registry
Trademark Filing- Madrid Protocol
Trademark Infringement and Litigation
Trademark Opposition
Trademark Prosecution
Translation & Interpretation
Translation of pharmaceutical documents
About company
Projects
Services
News
Team
Testimonials
Q & A
Contact
About original
Calculation of PDE and NOAEL
Cart
Checkout
Checkout-Result
Cleaning Validation and MACO calculation
Contact original
Copyright Filing in India and USA
Copyright Infringement Strategy
Copyright Litigation
Copyright Opposition
Copyright TM-C certificate prosecution
Country-Specific Trademark Search
Deficiencies management
Design Filing in India and USA
Design Infringement Analysis
Design Litigation
Design patent filing in the USA
Donation Confirmation
Donation Failed
Donor Dashboard
Drafting and submission management of PSUR, PBRER, PADER, Clinical Overview and DSURs: Comprehensive Pharmacovigilance Service packages for ROW region
eCTD/NEES publication services
Establishment of PSMF and drafting of Risk management plan
FTO Report
Gap Analysis
Home
Home Page
Infringement Analysis Report
Legal Notice and Seizures
Lifecycle maintenance: variations (Type IA, IB, II), renewal, and MA transfer, ‘sunset clause’ exemptions package, withdrawal
Literature search -Global/local literature search and review for reports of adverse events for all types of products, using standard terms
Local regulatory support
MA duplication procedure
MAA dossier – review and compilation of modules 1 to 5
Monitoring of literature for aggregated reports and safety information
My account
Patent Drafting and Filing before Patent Registry
Patent Infringement Suits and Litigation
Patent Prior Art Search
Patents
PCT Application Filing
Pct National Phase Application Prosecution
Pharmacovigilance
Post Grant and Pre Grant-Oppositions
Preparation of Toxicology reports
Product information preparation – SPC, PIL and Labelling
Products
Readability Testing and Bridging report
Regulatory due diligence and strategy
Regulatory Services
Regulatory services for specific countries e.g. LATAM, CIS + ex members, ASEAN, South Africa, ANZ, Botswana, Switzerland, etc.
Sample Page
Scientific and medical writing: Drafting of Clinical/Non-clinical report or overview, narrative, IMPD with all regulatory compliance of EMA/any country
Shop
Signal detection
Toxicology
Trademark
Trademark Filing before various Trademark Registry
Trademark Filing- Madrid Protocol
Trademark Infringement and Litigation
Trademark Opposition
Trademark Prosecution
Translation & Interpretation
Translation of pharmaceutical documents
About company
Projects
Services
News
Team
Testimonials
Q & A
Contact
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