@extends('FrontEndLayouts.frontApp')
@include('FrontEndLayouts.globalJqueryAjaxFunction')
@section('content')
    <!-- Breadcrumb Area -->
    <section class="breadcrumb-area text-center">
        <div class="container">
            <div class="row">
                <div class="col-md-12">
                    <h2>Phase II & Phase III Clinical Trials</h2>
                </div>
            </div>
        </div>
    </section>
    <!-- End Breadcrumb Area -->

    <section class="welcome-area">
        <div class="container">
            <div class="row">
                <div class="col-md-6" style="margin-top: -8px;">

                    <div class="welcome-box">
                        {{-- <h4>Welcome To KYABRS</h4> --}}
                        {{-- <img src="{{ URL::asset('frontEndAssets/images/heartbeat.png') }}" alt=""> --}}
                        <p>
                            Our in-house medical, regulatory and operational experts work collaboratively to support your
                            Phase IIb-III clinical trials as many moving parts go into Phase II and III clinical trials.
                            <br>

                            Our teams help eliminate delays by leading the way from recruitment strategies, medical writing,
                            and clinical logistics, all the way through the regulatory process.
                            <br>
                            We combine scientific leadership with disciplined execution, global access to patients, and
                            local and global regulatory expertise to accelerate your compound to approval.
                        </p>

                        <h5 style="color: black">Our Comprehensive Services for Accelerating Clinical Research</h5>
                        <ul class="order-list" style="text-align: justify;">
                            <li> Our expert physicians team provide strategic direction for
                                study design, train operations staff, provide medical monitoring, work with primary
                                investigators.</li>
                            <li> Strategic regulatory leadership guides trial design and
                                execution recommendations and meet with regulatory agencies.</li>
                            <li> Dedicated global regulatory submissions teams experienced in
                                key therapeutic and specialty area trial application processes and site start-up.</li>
                            <li> Proprietary, integrated clinical study management technology
                                platform facilitates efficient execution of global trials.</li>
                            <li> Experienced in Data Safety Monitoring Committee management.
                            </li>
                            <li> Provides ongoing statistical support.</li>

                            <li> Detailed site selection processes, ongoing tracking and site
                                communication to maintain trial timelines.</li>
                            <li> Extensive and rigorous in-house training program.</li>

                        </ul>
                        {{-- <a href="#">Read More</a> --}}
                    </div>
                </div>
                <div class="col-md-6">
                    <div class="about-image">
                        <img src="{{ URL::asset('frontEndAssets/images/Clinic-C.JPG') }}" alt="" class="img-fluid">
                    </div>
                </div>
            </div>
        </div>
    </section>
@endsection