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

Last Updated: December 31, 2025

Profile for Croatia Patent: P20141047


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Croatia Patent: P20141047

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.

Detailed Analysis of the Scope, Claims, and Patent Landscape for Croatia Patent HRP20141047

Last updated: August 13, 2025


Introduction

Croatia Patent HRP20141047, granted in 2014, represents an innovative claim within the pharmaceutical sector, reflecting Croatia's engagement with drug patenting. This patent’s detailed analysis—covering scope, claims, and the broader patent landscape—is crucial for assessing its commercial potential, competitive positioning, and legal robustness. This review synthesizes key aspects through technical, legal, and market perspectives, providing insights relevant for stakeholders such as pharma companies, patent attorneys, and R&D strategists.


Patent Overview and Context

HRP20141047 addresses a novel pharmaceutical formulation or compound, with its exact nature detailed in the patent specification (not provided directly here). Given Croatia’s patent landscape—characterized by rigorous national and international patent standards—this patent aims to secure exclusive rights over specific drug compositions, methods of manufacturing, or therapeutic indications.

Croatia recognizes patents linked to pharmaceuticals via the European Patent Convention (EPC) and maintains strict criteria for patentability—novelty, inventive step, and industrial applicability. The patent's scope hinges on these factors, which are consistent with regional and international patent laws.


Scope of the Patent

Legal Scope and Boundaries

The scope of Croatian patent HRP20141047 is primarily defined by its claims—declarative statements that delineate the boundaries of patent protection. These claims determine what variations or embodiments the patentist explicitly seeks to control. There are generally two types:

  • Independent Claims: Broader, foundational claims defining the core invention.
  • Dependent Claims: Narrower, elaborating on specific embodiments or enhancements.

Without access to the exact claims, typical scope in pharmaceutical patents includes:

  • Chemical Composition: Specific molecules, salts, stereoisomers, or derivatives.
  • Method of Preparation: Unique synthetic routes or manufacturing procedures.
  • Therapeutic Use: Particular indications or doses.
  • Formulation: Specific excipients, delivery mechanisms, or physical forms.

In this case, the patent likely covers a unique drug molecule, a specific formulation, or a novel method of synthesis, which enables differentiation from prior art.

Technical Scope

The technical scope might encompass:

  • Compound Structure: Exact chemical formulae and stereochemistry.
  • Preparation Techniques: Innovative synthesis pathways.
  • Use Cases: Targeted diseases or symptoms.
  • Delivery Systems: Extended-release formulations or delivery devices.

The comprehensiveness of these claims impacts enforceability and license potential. Broad claims afford greater protection but risk invalidation for lack of novelty or inventive step, while narrow claims limit scope but enhance defensibility.


Claims Analysis

Claim Characteristics

Croatian patents generally employ claims constructed to balance breadth and clarity:

  • Novelty & Inventive Step: Ensured through specific structural features or process innovations.
  • Clarity: Claims are precisely drafted to withstand legal scrutiny.
  • Support: Backed by detailed description and examples demonstrating feasibility.

Typical Claim Types in Pharmaceutical Patents

  1. Compound Claims: Cover the chemical entity’s structural formula.
  2. Method Claims: Encompass processes for synthesizing or administering the drug.
  3. Use Claims: Define novel therapeutic applications.
  4. Formulation Claims: Cover specific drug delivery systems.

Example (Hypothetical)

  • "A compound with the structure of Formula I, or its pharmaceutically acceptable salt, characterized by..."
  • "A method for treating [disease] comprising administering an effective amount of the compound..."

The scope of such claims generally hinges on how narrowly or broadly the structure or method is defined.

Claim Limitations and Strategies

In Croatia, claims avoiding prior art are essential. Overly broad claims risk invalidation, whereas overly narrow claims may open avenues for competitors to design around. Strategic claim crafting involves:

  • Incorporating unique molecular features.
  • Defining innovative synthesis steps.
  • Restricting claims to specific doses or formulations.

Patent Landscape in Croatia and Europe

Croatian Patent Environment

Croatia’s pharmaceutical patent landscape is intertwined with European Patent Office (EPO) standards, given their accession to the EPC. Croatian patents benefit from the same substantive examination procedures, ensuring high-quality protection.

Key Characteristics:

  • Patentability Requirements: Strict novelty, inventive step, such as those applied for other pharmaceutical patents.
  • Patent Term: 20 years from filing, contingent upon maintenance fees.
  • Enforcement: National courts uphold patent rights; enforcement mechanisms align with EU standards.

European Patent Influence

Many Croatian patents are originated from or complemented by European patents—either through direct applications or national phase entries. The central European patent system encourages:

  • EPC Applications: Allowing one application to cover multiple European countries, including Croatia.
  • Patent Families: Protecting innovations across jurisdictions.

The patent landscape includes:

  • Major Players: Multinational corporations, biotech firms, and local entities.
  • Technological Focus: Anti-inflammatory agents, oncology drugs, cardiovascular therapies, reflecting regional healthcare needs.

Prior Art and Patent Challenges

Croatia’s patent system rigorously assesses prior art, which includes:

  • Existing medicinal compounds.
  • Scientific publications.
  • Previous patents from Croatia, Europe, and globally.

Patent opposition and invalidity procedures are possible, emphasizing the importance of robust, well-drafted claims.

Comparative International Landscape

Compared to other jurisdictions, Croatia’s patent landscape for pharmaceuticals is highly harmonized with European standards. Anticipated overlaps with German, French, and UK patents are common, requiring strategic patentability analyses before filings.


Implications for Stakeholders

  • Patent Holders: Should focus on crafting specific, inventive claims that withstand European and Croatian scrutiny, leveraging the national and regional framework.
  • Competitors: Need to perform detailed freedom-to-operate (FTO) analyses, considering Croatian patent claims and potential invalidation strategies.
  • R&D Entities: Can explore licensing or partnership opportunities around the claims, especially if the patent protects promising drug candidates.

Key Takeaways

  • Croatian patent HRP20141047 likely claims a specific drug compound, formulation, or method, with scope defined by its claims’ wording.
  • Robust claim drafting is crucial to balancing broad protection with validity, especially considering prior art.
  • The Croatian patent landscape is aligned with European standards, emphasizing high-quality examination and enforcement.
  • Navigating the patent landscape requires understanding both national and European protections to safeguard investments.
  • Strategic claim amendments and prosecution efforts enhance patent strength, ensuring market exclusivity and licensing opportunities.

FAQs

1. How does Croatian patent law influence pharmaceutical patent strategies?
Croatian patent law, aligned with EPC standards, emphasizes rigorous novelty and inventive step requirements, prompting applicants to develop highly specific claims and detailed descriptions to secure enforceable rights.

2. Can a Croatian patent be enforced internationally?
Croatia is a member of the EPC, facilitating the extension of patent rights via European patents. For global enforcement, patentees typically pursue filings in jurisdictions of interest, leveraging bilateral agreements or international treaties.

3. What are common pitfalls in claiming pharmaceutical inventions in Croatia?
Vague or overly broad claims risk invalidation, failing to demonstrate inventive step, or overlapping with prior art. Precise, well-supported claims are vital for robust protection.

4. How does patent landscape competition impact drug development in Croatia?
Intense competition necessitates innovative, non-obvious inventions with solid claims. Understanding existing patents prevents infringement and informs licensing strategies.

5. What are key considerations when filing new pharmaceutical patents in Croatia?
Applicants must ensure claim novelty, define inventive features clearly, and conduct thorough prior art searches to avoid invalidation risks, alongside timely maintenance to preserve patent rights.


References

[1] Croatian Intellectual Property Office (HIPO). Patent Law and Guidelines.
[2] European Patent Office (EPO). Guidelines for Examination.
[3] WIPO. International Patent Cooperation.
[4] Croatian Patent Database. Prior Art Search Reports.

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.