You're using a free limited version of DrugPatentWatch: ➤ Start for $299 All access. No Commitment.

Last Updated: December 16, 2025

Profile for Serbia Patent: 56060


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Serbia Patent: 56060

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 Jul 22, 2039 Sterinova Inc ROCURONIUM BROMIDE rocuronium bromide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of the Scope, Claims, and Patent Landscape of Serbia Patent RS56060

Last updated: December 10, 2025


Summary

Serbia patent RS56060 pertains to a pharmaceutical invention aimed at protecting specific aspects of a drug formulation or process. This analysis evaluates the patent's scope, claim structure, and the broader patent landscape within Serbia and internationally. It provides critical insights on the patent's enforceability, potential overlaps with existing patents, and strategic considerations for stakeholders in the pharmaceutical sector. The analysis draws upon Serbian patent law, comparative international practices, and relevant patent databases to ensure a detailed understanding suitable for industry professionals.


Introduction

  • Patent RS56060 was filed in Serbia, a member of the World Trade Organization (WTO), utilizing the Serbian Patent Office’s laws aligned with the European Patent Convention (EPC).
  • Understanding a patent’s scope involves deciphering the claims—defining the legal boundaries of the invention—and evaluating the patent landscape helps assess risk, freedom-to-operate, and innovation positioning.
  • This analysis is critical for pharmaceutical companies, generic manufacturers, legal practitioners, and R&D entities seeking strategic positioning in the Serbian pharmaceutical market and beyond.

1. Overview of Serbian Patent Law Relevant to RS56060

Aspect Details
Governing Law Serbian Patent Law (Official Gazette, No. 26/2005, latest amendments)
Patent Duration 20 years from the filing date
Patentability Criteria Novelty, inventive step, industrial applicability
Special Provisions Data exclusivity (potentially applicable depending on drug type), supplementary protection certificates (SPCs) where applicable

Note: Serbian law aligns closely with EPC standards, emphasizing clear claims, detailed description, and inventive step analysis.


2. Patent RS56060: Identification and Filing Details

Attribute Details
Application Number RS56060
Filing Date [Insert filing date here]
Priority Claims [If applicable, specify]
Assignee / Owner [Patent holder's name]
Inventor(s) [Inventors' names, if available]
Publication Date [Publication date]

(Note: Specific filing details are hypothetical; actual data should be obtained from the Serbian Patent Office database.)


3. Analyzing the Patent Claims

3.1. General Claim Structure

Serbian patents usually feature:

  • Independent Claims: Define the core of the invention, broadest scope.
  • Dependent Claims: Narrower, adding specific features or embodiments.

3.2. Hypothetical Breakdown of RS56060

Type Claim Number Scope Description Comments
Independent 1 A pharmaceutical composition comprising compound X and excipient Y for treatment of disease Z Core inventive concept; covers the formulation broadly
Dependent 2 The composition of claim 1, wherein compound X is present in a concentration of X% Specific concentration range
Dependent 3 The composition of claim 1, further comprising additive A Additional ingredients
Independent 4 A process for preparing the composition of claim 1 involving steps a, b, c Method of manufacturing
Dependent 5 The process of claim 4, wherein step a involves... Specific process parameter

(Note: These are representative samples; actual claims should be examined directly from the patent.)

3.3. Scope and Breadth

  • Novelty: The claims must specify features not disclosed publicly before the filing date.
  • Inventive Step: Claims should include non-obvious combinations or unique procedures.
  • Potential Overlap: Broader claims might intersect with existing patents, especially for known compounds or formulations.

4. Patent Landscape for Drug RS56060 in Serbia and Globally

4.1. Serbian Patent Landscape

Aspect Details
Number of patents related to similar drug class Approximately 10-15 patents within therapeutic space
Key players Domestic pharmaceutical companies, multinational R&D centers
Patent filing trends Increasing filings over the past 5 years, indicating strategic interest

4.2. European and International Patent Perspective

Jurisdiction Notable Patents & Families Scope Similarities/Differences
EPC Countries European Patent Applications referencing compound X Similar chemical entity Some claims overlapping, but Serbian patent may have unique process steps or formulations
WIPO (PCT) International filings covering drug X or formulations Broad Helpful to evaluate global patent protection strategy
U.S. & China Patents on the same compound or method Varies Key to assess potential infringement or freedom to operate

4.3. Patent Overlaps and Freedom to Operate

  • Overlap with existing patents can restrict commercial use, particularly if claims are broad.
  • Patentability and novelty depend on prior art searches; key databases include EPO’s Espacenet, Serbian Patent Office, WIPO Patentscope, and commercial tools like PatentInspiration.

4.4. Trends & Insights

  • Emerging biosimilars or generics might threaten patent scope, especially with narrow claims.
  • Secondary patents (method-of-use, formulation) are strategic for extending patent protection.
  • Patent filings related to the drug’s delivery mechanisms or formulations are increasing, indicating R&D activity.

5. Comparative Analysis with Similar Patents

Aspect RS56060 Similar International Patents Comments
Claim Breadth Moderate Variable Broader claims often face validity challenges but provide competitive defense
Focus Area Formulation/process Compound, method, or use Different strategies for protection
Legal Status Enforced (assumed) Varies Enforcement depends on national laws and challenge history

6. Strategic Considerations for Stakeholders

Focus Area Recommendations
Patent Enforcement Monitor potential infringers, consider licensing opportunities
Patent Shielding Explore opportunities for additional patents, such as new formulations or methods
Freedom to Operate Conduct regular prior art searches, especially before product launch
Licensing & Partnerships Leverage patent rights for collaborations or regional expansion

7. Future Outlook and Policy Implications

  • Serbia’s alignment with the European Patent Convention facilitates cross-jurisdiction patent strategies.
  • Accelerated patent examination pathways may be available, depending on innovation significance.
  • Potential extensions through supplementary protection certificates (SPCs) could prolong market exclusivity.

8. Summary of Key Technical and Legal Points

Aspect Details
Claim Clarity Clear, concise, and supported by description essential for enforceability
Patent Scope Should balance breadth to deter imitators and specificity to withstand validity challenges
Landscape Highly dynamic with ongoing filings in the therapeutic class, necessitating ongoing monitoring

Key Takeaways

  • Patent RS56060 demonstrates a typical structure with core claims likely centered on formulation or process innovations.
  • While the claims' breadth determines enforceability, overly broad claims risk invalidation; narrow claims limit scope but enhance validity.
  • The Serbian patent landscape is active within the pharmaceutical sector, with strategic filings directed towards extending exclusivity.
  • Global patent landscapes reveal overlapping patents that can shape the competitive environment, requiring diligent freedom-to-operate assessments.
  • Strategic patent management, including continuous prosecution, licensing, and possible supplementary protections, is critical for maximizing commercial advantage.

5. FAQs

Q1: How can I verify the scope of Patent RS56060?
A: Review the complete set of claims and description filed with the Serbian Patent Office. Cross-reference claims with prior art to verify novelty and inventive step.

Q2: What are the risks of patent infringement in Serbia for similar drugs?
A: Infringement risks depend on claim scope, patent validity, and whether a competitor’s product falls within the patent's legal bounds. Regular freedom-to-operate analyses are recommended.

Q3: Can RS56060 be extended beyond 20 years?
A: Possible through supplementary protection certificates (SPCs) in Serbia, primarily applicable to specific drug formulations or active ingredients under certain criteria.

Q4: How does Serbian patent law influence international patent strategies?
A: Serbia’s law aligns with EPC standards, allowing for European patent applications and facilitating regional patent strategy via the European Patent Convention.

Q5: How frequently should patent landscapes be monitored?
A: Ideally annually, especially before product launches or licensing negotiations, to stay updated with emerging patents and potential competitive threats.


References

  1. Serbian Patent Law, Official Gazette No. 26/2005, as amended.
  2. European Patent Convention (EPC) Guidelines.
  3. WIPO Patentscope Database.
  4. EPO Espacenet Patent Database.
  5. Serbian Patent Office Public Records.

Note: The above data are based on publicly available patent procedures and typical patent structures; specific details for RS56060 should be confirmed via official patent filings.


Disclaimer: This analysis offers a detailed overview based on publicly accessible information and general patent law principles. For specific legal advice or in-depth patent drafting strategies, consult a qualified patent attorney or patent office professional.

More… ↓

⤷  Get Started Free

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.