ROI-Driven paid search optimization
Our relationship with you relies on getting results, and paid search marketing results are measured in ROI. Each and every day, our primary focus is building ROI by interpreting real data and creating campaigns that convert. This includes:
- Keyword and competitor research
- SKAGS (single keyword ad groups)
- Negative keyword pruning
- Ad copy optimization
- Landing page creation & optimization
- Search engine retargeting
Zoe global
How our regulatory writing services can help meet your goals?
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Enhancing Regulatory Compliance and Success in Healthcare and Pharmaceuticals with Zoe Global
Zoe Global is your trusted partner when it comes to achieving your regulatory goals. Our expert team of regulatory writers is dedicated to crafting documents that meet the highest industry standards and compliance requirements. We understand the intricate landscape of regulatory affairs and leverage our extensive knowledge to ensure that your submissions are accurate, comprehensive, and compelling. Whether you need assistance with clinical trial documentation, marketing authorization applications, or post-market surveillance reports, our services can streamline the regulatory process, saving you time and resources while helping you navigate the complex world of regulatory compliance with confidence. Partner with Zoe Global to unlock the potential for successful regulatory submissions and ultimately achieve your goals in the ever-evolving healthcare and pharmaceutical sectors.
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Get a team of certified Google Adwords / SEM specialists who have a minimum of 2 years experience managing various SEM campaigns locally. We help you create the perfect combination of strategy and implementation to ensure we achieve your goals.
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what you get
What is included in our regulatory writing services?
When you partner with Zoe Global, you’ll gain access to our full range of regulatory writing services. These services have been meticulously designed to enhance every aspect of your drug approval strategy, including:
Clinical Study Report (CSR)
The process of creating a Clinical Study Report (CSR) at Zoe Global involves a meticulous and multifaceted approach. To initiate this crucial phase of clinical research, several key documents are essential. First and foremost, the study protocol lays the foundation, outlining the study design, objectives, and methodology. Patient data, including case report forms (CRFs), electronic data capture (EDC) records, and tables, listings, figures (TLFs) provide the raw material for the CSR. Statistical analysis plans and datasets play a pivotal role in data interpretation and analysis. Finally, ethics committee approvals ensure compliance with all necessary guidelines and regulations, culminating in the comprehensive and scientifically rigorous CSR. Throughout the process, there is a rigorous quality control mechanism in place to guarantee the highest standards of accuracy and compliance. Collaboration and communication with clients play a pivotal role, as we work closely to understand their specific objectives and tailor the CSR accordingly. This collaborative approach, combined with our team’s deep expertise and commitment to excellence, ensures the creation of CSRs that are not only regulatory compliant but also effectively communicate the trial’s findings, ultimately contributing to the advancement of medical knowledge and patient care.
Clinical Study Protocol (CSP)
Creating a Clinical Study Protocol (CSP) at Zoe Global involves a systematic and detail-oriented approach. Our experienced team of medical writers collaborate closely to design a protocol that adheres to regulatory standards and aligns with the specific goals of the study. This process includes defining the study objectives, patient eligibility criteria, study endpoints, and methodology for data collection and analysis. Ethical considerations and patient safety are paramount, and protocols are developed in accordance with ethical guidelines and regulations. Throughout this process, there is continuous input and feedback from our clients to ensure that their research goals are met. The CSP serves as the roadmap for the entire clinical trial, providing a clear and comprehensive plan that ensures the study is conducted with integrity, precision, and adherence to regulatory requirements.
Informed Consent Form (ICF)
The creation of an Informed Consent Form (ICF) at Zoe Global is a meticulous and patient-centric process. Our team of experienced professionals, including medical writers and legal experts, collaborate to craft ICFs that are clear, concise, and compliant with regulatory standards. We begin by thoroughly understanding the study and its potential risks and benefits. We then translate complex medical and legal information into language that is easily comprehensible to participants, ensuring they are fully informed about their participation. The ICF also emphasizes the voluntary nature of participation, respecting the autonomy and rights of each participant. Client collaboration and ethical considerations are integral to this process, and we strive to strike a balance between regulatory compliance and patient-friendly communication. The result is an ICF that prioritizes patient understanding and protection, reflecting Zoe Global’s commitment to ethical research practices.
Investigator’s Brochure (IB)
Preparing an Investigator’s Brochure (IB) at Zoe Global is a meticulously executed process that combines scientific expertise and regulatory adherence. Our specialized team of medical writers and researchers collaborate to compile comprehensive, up-to-date information about the investigational product. This includes data on its pharmacology, safety, and efficacy, drawing from preclinical and clinical studies. The IB is structured in compliance with regulatory guidelines, ensuring that it provides a clear and organized resource for investigators conducting clinical trials. Constant communication with our clients is vital to align the IB with their specific research objectives. The resulting Investigator’s Brochure is a vital tool that aids in the safe and ethical conduct of clinical trials, enabling investigators to make informed decisions and protect the well-being of study participants.
Common Technical Document (CTD) modules
Preparing Common Technical Document (CTD) modules 2.5, 2.7.3, and 2.7.4 at Zoe Global is a highly specialized and detail-oriented process. Our team of regulatory writers and experts meticulously compile and organize the necessary information for these modules, which are critical components of regulatory submissions. Module 2.5 focuses on clinical summaries, requiring a comprehensive and coherent presentation of clinical trial data, while modules 2.7.3 and 2.7.4 pertain to clinical study reports and individual patient data respectively. We adhere rigorously to international regulatory guidelines, ensuring the accuracy, completeness, and adherence to regulatory requirements. Throughout this process, close collaboration with clients is maintained to ensure that these CTD modules align precisely with their regulatory objectives and needs. The outcome is a meticulously prepared set of CTD modules that contribute significantly to successful regulatory submissions, reflecting Zoe Global’s commitment to excellence in regulatory writing and compliance.
Lay summaries
Our team of skilled medical writers work diligently to distill complex scientific and medical information from clinical trial documents into plain language that can be easily understood by the general public. This process involves careful review of the study’s results, benefits, and risks, with a strong emphasis on ensuring clarity and transparency. Client collaboration is integral, as we strive to align Lay Summaries with their specific objectives and requirements. The end result is a Lay Summary that empowers patients and the public with clear, accessible information about clinical trials, enabling them to make informed decisions and fostering transparency in medical research. Zoe Global’s commitment to ethical and effective communication shines through in this critical aspect of our services.
Patient Narratives
At Zoe Global, our dedicated and experienced team of medical writers takes meticulous care in the thorough examination and analysis of adverse event data. This rigorous process enables us to construct patient narratives that offer a precise, comprehensive, and compassionate account of each individual’s medical journey. In crafting these narratives, we prioritize the utmost sensitivity and respect for patient privacy, ensuring that the information shared strictly adheres to stringent regulatory guidelines.
Our collaborative approach extends to our valued clients, as we work closely with them to tailor these narratives to align seamlessly with their specific reporting requirements and objectives. By doing so, we not only meet regulatory compliance standards but also provide a valuable tool for understanding the profound impact of adverse events on patients’ lives. This underscores our unwavering commitment to patient-centricity and ethical reporting, reinforcing Zoe Global’s standing as a trusted partner in the healthcare industry. Through our diligent and compassionate efforts, we contribute to a safer and more patient-focused healthcare landscape.
Synopsis
The process of preparing synopsis at Zoe Global is a highly structured and detail-oriented endeavor. Our team of regulatory writers and experts meticulously extract and distill key information from comprehensive regulatory documents, such as CSRs and clinical trial protocols. These synopsis provide a concise overview of the essential details, including study objectives, methodology, and key findings, all while adhering to regulatory guidelines and industry best practices. Client collaboration is central to ensure that the synopsis align with their specific needs and objectives. The result is a well-structured and information-rich synopsis that serves as a valuable tool for regulatory submissions and decision-making, showcasing Zoe Global’s commitment to precision and excellence in regulatory writing.
Responses to Regulatory Authority Questions
The process of preparing responses to inquiries from regulatory authorities represents a multifaceted and strategic undertaking, one that demands the utmost diligence and expertise. At Zoe Global, we approach this task with a meticulous and comprehensive methodology, which begins with an in-depth analysis of the questions and concerns articulated by regulatory authorities.
Our commitment to excellence in this endeavor is unwavering, as we strive to provide our clients with responses that are scientifically robust, well-informed, and tailored to effectively address the regulatory inquiries. We do this while ensuring strict adherence to established regulatory guidelines and best practices.
Collaboration lies at the heart of our approach, and we work closely with our clients to deliver responses that align perfectly with their specific needs and objectives. These responses are not just technical documents; they are crafted with precision, clarity, and a profound understanding of the intricate regulatory landscape and the unique characteristics of the client’s product or study. Our ultimate goal is to create responses that are not only compliant with regulatory standards but also compelling. We aim to present a strong and persuasive case that supports the approval or compliance of the product in question. This involves weaving a narrative that articulates the benefits and safety of the product, as well as addressing any concerns in a comprehensive and scientifically sound manner.
Clinical Documentation
Our team of highly skilled medical writers and subject matter experts come together in a collaborative effort to compile, meticulously organize, and effectively communicate intricate clinical data. This multifaceted undertaking entails the assimilation of information from a diverse array of sources, ranging from comprehensive clinical trial reports and intricate study protocols to detailed patient records. Our mission is to transform this wealth of data into a coherent, well-structured, and comprehensive representation.
This process places a significant emphasis on attention to detail, as we meticulously ensure that every piece of data is accurate, relevant, and aligned with the stringent regulatory requirements governing clinical documentation. Furthermore, our partnership with our clients is integral to our operations, as we work closely to understand their specific needs and objectives, ensuring that the documentation we produce is customized to their unique vision.
Whether it is the development CSRs, Protocols, or IBs, our overarching goal is to deliver clinical documentation of the highest quality. We not only guarantee that our work meets the rigorous standards set by regulatory authorities but also that it effectively communicates the intricate scientific and medical aspects of the research at hand. By doing so, we contribute significantly to the advancement of healthcare and the expansion of medical knowledge, playing an instrumental role in enhancing the overall landscape of medical research and patient care.
Creating Success
What makes our paid search management services so effective?
Match search intent at every touchpoint
Picking the right keywords will only get you so far. We understand how to match the search intent of your target keywords with ad copy, CTAs, and landing pages that turn clicks into ROI.
Experienced PPC management
How do you know what works if you’ve never gotten results before? Our paid search managers have years of experience managing successful campaigns in a variety of industries. And we have the happy clients to back it up.
Google Premier Partnership
Working with a Google Partner agency gives you a leg up. Not only are we certified in all types of Google advertising, but we also get access to direct support and other resources provided by Google. Your campaigns benefit directly from this exclusive insider knowledge.
“Numerique PPC service is light years ahead of the competition because of their intelligent, specialized and courteous account managers.”
Director of Marketing
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The proof is in the numbers
Why paid search Ads can bring in the numbers
38%
of growth rate in brand awareness for businesses that start doing Search Ads
100%
of total clicks on search results page are Search Ads, serving as proof that a dependence on SEO alone limits your potential for more traffic and leads.
82%
of clicks on Search Ads are more likely to buy, making for better leads
FAQ
FAQs about paid search management
Looking to learn more about paid search management for your business? Browse our FAQs:
Paid search is a digital marketing strategy that involves online ads that appear at the top of search engine results pages (SERPs). Paid search ads typically look similar to organic search listings but have a label that distinguishes them as ads.
With paid search management services, you can expect a dedicated team of experts who will meticulously review and analyze your campaigns, ensuring that they align with your business objectives. Through continuous optimization, they will fine-tune your advertisements to maximize their effectiveness, reaching the right audience at the right time.
When it comes to paid search ads, Google Ads serves as a prime example of how the process works. Google Ads allows advertisers to bid on specific keywords they want their ads to appear for. When a user conducts a search on Google, the platform uses various factors such as keywords, ad settings, bids, and ad quality score to determine which ads to display.
Paid search can indeed be a valuable addition to your marketing strategy for several reasons: Audience Research, Precise Targeting, Quick Results, Bottom-of-the-Funnel Leads, Supplementing Organic Search Results. By leveraging the advantages of paid search, businesses can effectively target their audience, generate qualified leads, achieve faster results, and enhance their overall online visibility and conversion rates.