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Atop Pharma Solutions
Your partner for all regulatory and translation 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
- 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