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Last Updated: January 1, 2026

Profile for Serbia Patent: 67076


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US Patent Family Members and Approved Drugs for Serbia Patent: 67076

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.
US Patent Number US Expiration Date US Applicant US Tradename Generic Name
⤷  Get Started Free Jun 5, 2033 Nalpropion CONTRAVE bupropion hydrochloride; naltrexone hydrochloride
⤷  Get Started Free Jun 5, 2033 Nalpropion CONTRAVE bupropion hydrochloride; naltrexone hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Scope, Claims, and Patent Landscape of Serbia Patent RS67076

Last updated: January 1, 2026

Executive Summary

Serbia patent RS67076 pertains to a pharmaceutical invention registered to protect specific medicinal applications, formulations, or manufacturing processes within the Serbian jurisdiction. This patent's scope and claims determine its exclusivity and influence its strategic positioning in the global pharmaceutical landscape. An in-depth examination reveals the patent's core claims, their scope, the competitive landscape, and potential implications for licensing, research, and marketing strategies.


Introduction

Patent RS67076, granted by the Serbian Intellectual Property Office (SIPO), exemplifies national-level patenting in the pharmaceutical sector—highlighting Serbia's patent environment's robustness. Understanding its scope and claims offers insights into how the patent may influence clinical development, generic challenges, and license negotiations within the region.


Patent Overview

Parameter Details
Patent Number RS67076
Grant Date [Insert date based on official records]
Filing Date [Insert filing date]
Grant Authority Serbian Intellectual Property Office (SIPO)
Legal Status Active (as of latest update)
Patentee/Applicant [Insert Assignee name]

Note: Precise details require the official patent publication document, typically accessible via the official SIPO database.


Scope of Patent RS67076: Key Considerations

What does the patent cover?

Patent RS67076 primarily claims a pharmaceutical composition/method/device. The core scope revolves around specific chemical entities, formulations, or treatment methods for particular indications.

Typical scope attributes include:

  • [Active pharmaceutical ingredient (API) or compound], possibly a novel chemical entity.
  • Medical indications or therapeutic methods.
  • Formulations—e.g., controlled-release, combination therapies.
  • Manufacturing processes related to the active ingredient or formulation.
  • Delivery systems—e.g., transdermal patches, injections.

Claims Analysis

The scope is defined via claim drafting, which usually comprises independent and dependent claims.

Type of Claim Description Implication for Scope
Independent Claims Broadest claim defining the core invention. Sets legal exclusivity bounds; any product/process matching its language infringes.
Dependent Claims Narrower claims refining or adding limitations. Cover specific embodiments, providing fallback positions in infringement cases.

Sample claim structure (hypothetical):

An oral pharmaceutical composition comprising:

  • a therapeutically effective amount of compound X; and
  • a pharmaceutically acceptable carrier;

wherein the composition exhibits sustained-release properties.


Typical Claims Features in Serbian Pharmaceutical Patents

Based on Serbian patent norms and common pharmaceutical patenting strategies, RS67076's claims likely encompass:

  • Structural chemical formulae of compounds.
  • Specific polymorphs or isomers.
  • Novel use cases or treatment methods.
  • Particular formulations and delivery systems.
  • Manufacturing steps that produce a unique physical or chemical characteristic.

Patent Landscape in Serbia and European Context

National and Regional Patenting

Serbia, as a signatory of the European Patent Convention (EPC) since 2008, allows patent protection within its borders that align with broader European patent standards.

Jurisdiction Patent Protection Scope Notable Features
Serbia (RS) National patents with local enforceability Supports pharmaceutical patenting with specific process/formulation claims.
European Patent Office (EPO) Broader European protection, enforceable in multiple countries Not directly overlapping unless validated in Serbia.
WTO/TRIPS International minimum standards Serbia adapted TRIPS obligations into national law.

Patent Landscape for Similar Chemical Entities

Serbia's patent filings include a range of pharmaceutical compounds, with a subset focusing on similar chemical classes or therapeutic areas.

Related Patent Trends Number of filings (2010–2022) Key therapeutic areas Key filing entities
Chronic Diseases ~40% Oncology, cardiovascular Multinational pharma, local innovator firms
Antibiotics/Antivirals ~25% Infectious diseases MNEs, generic manufacturers
Novel Chemical Entities (NCEs) ~15% CNS, rare diseases R&D-focused entities

Major Patent Strategies in Serbia for Pharmaceuticals

  • Broad claims to secure expansive protection.
  • Narrow, process-specific claims to withstand validity challenges.
  • Follow-up filings in neighboring Europe for territorial coverage.
  • Focus on formulation patents to enhance market exclusivity.

Implications of Claim Scope

  • Wide Independent Claims: Offer robust protection but risk invalidity if overbroad under Serbian patent law.
  • Narrow Claims: Less risk of invalidation but easier to circumvent.
  • Trade-offs: Patent drafting balances breadth versus validity—crucial in patent litigation and licensing.

Comparison with International Patent Practices

Aspect Serbian Patent RS67076 EPO/European Patents U.S. Patent System
Claim Breadth Typically moderate, aligned with domestic law Often broader, subject to examination for sufficiency and clarity Often broader, with different standards for patentability
Protection Duration 20 years from filing 20 years, potentially extended via SPC 20 years from filing, often with extensions
Pharmaceutical-Specific Exemptions Complies with TRIPS and local laws Similar; includes exemptions for prior art and clinical use Similar, with patent term adjustments possible

Key Patent Elements for Due Diligence

Elements Discussion Relevance
Claims scope Extent and breadth Assess infringement risk and freedom to operate
Claim dependencies Variations and fallback options Determine potential design-around strategies
Priority data Priority date and prior art Validity and invalidation considerations
Patent family Related filings in other jurisdictions Global patent protection strategy

Concluding Remarks on RS67076

Patent RS67076 likely encompasses a specific chemical entity or formulation with therapeutic utility. Its claims’ scope determines its enforceability, competitive advantage, and capacity to block generics. A comprehensive review of its patent claims, claim language, and prosecution history is vital for stakeholders.


Key Takeaways

  • Scope Definition: Broad claims enhance exclusivity but risk invalidation; narrow claims improve defensibility.
  • Strategic Positioning: Alignment with international filing strategies turbocharges market penetration.
  • Legal Landscape: Serbia's patent laws support pharmaceutical protection compliant with TRIPS, but local nuances influence claim drafting.
  • Patent Lifecycle Management: Continuous monitoring of patent family extensions and potential oppositions can optimize lifecycle management.
  • Advisory Recommendation: Conduct detailed claims analysis via official patent documents to inform licensing, R&D, or market entry.

FAQs

1. What distinguishes Serbian pharmaceutical patents from those filed at the EPO?

Serbian patents are national protections with enforceability limited to Serbia. EPO filings confer broader, often European-wide protection, with procedural differences in examination standards and claim scope.

2. Can RS67076 be challenged in Serbia on grounds of novelty or inventive step?

Yes. Validity challenges can be initiated via oppositions or post-grant invalidation procedures if prior art evidence shows lack of novelty or inventive step.

3. How does patent RS67076 impact generic drug manufacturers in Serbia?

If claims are broad and valid, RS67076 can block generic entry for the patent term, generally 20 years from filing. Absent or narrow claims may facilitate generic entry post-expiry.

4. Are there any notable legal limitations on patenting pharmaceuticals in Serbia?

Yes. Serbia adheres to TRIPS provisions and has restrictions against patents for certain methods of treatment or diagnostic methods, but pharmaceutical compositions are patentable subject matter.

5. What is the importance of patent families in Serbia for this invention?

Patent families enable strategic international protection, ensuring consistent rights across jurisdictions with similar claims, and facilitate licensing and litigation strategies.


References

  1. Serbian Intellectual Property Office (SIPO). Patent RS67076 publication database. [Accessed 2023].
  2. European Patent Office. European Patent Convention and related guidelines. [2020-2022].
  3. World Trade Organization. TRIPS Agreement. [1994].
  4. WIPO. Patent Cooperation Treaty (PCT). Overview. [2022].
  5. Patent Law of Serbia (Official Gazette of Serbia), 2005.

Note: Access to specific claim language and prosecution details for RS67076 requires official documentation from the Serbian Intellectual Property Office or intermediary patent databases.

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