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Atop Pharma Solutions
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Atop Pharma SolutionsAtop Pharma Solutions
+91 98981 24444info@atoppharmasolutions.com
  • 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
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  • Copyright Opposition
  • Copyright TM-C certificate prosecution
  • Country-Specific Trademark Search
  • Deficiencies management
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  • Design Infringement Analysis
  • Design Litigation
  • Design patent filing in the USA
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  • Donation Failed
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  • 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
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  • 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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  • Location:
    1015, Shivalik Satyamev, Ambli Bopal Flyover Junction , Ahmedabad - 380058, Gujarat.
    A803, Haosheng Buiding, Maidi Raod, Huizhou City, Guangdong Province, China.
  • Phone number:
    +91 98981 24444
    +91 27174 89575
    +86 18127715266
  • E-mail:
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